3950-21-8

Usage

Uses

Used in the Chemical Industry:
(R,S)-Pentane-2,4-diol is used as a solvent for various chemical processes due to its ability to dissolve a wide range of substances. Its solubility properties make it a versatile component in the chemical industry.
Used as an Intermediate in Organic Synthesis:
(R,S)-Pentane-2,4-diol serves as an intermediate in the synthesis of more complex organic compounds. Its reactive hydroxyl groups facilitate further chemical reactions, allowing for the creation of a diverse array of products.
Used in the Production of Polymers and Adhesives:
As a component in the production of polymers and adhesives, (R,S)-Pentane-2,4-diol contributes to the formation of strong and durable materials. Its involvement in polymerization reactions helps create polymers with specific properties for various applications.
Safety:
(R,S)-Pentane-2,4-diol is considered to be relatively low in toxicity and is not known to have any significant biological effects. However, it is essential to handle this chemical with care and to follow appropriate safety precautions to ensure the well-being of individuals working with it.

InChI:InChI=1/C5H12O2/c1-4(6)3-5(2)7/h4-7H,3H2,1-2H3

Upstream product

• 4161-60-8 4-hydroxypentan-2-one 
• 123-54-6 acetylacetone 
• 17615-19-9 3,4-pentadien-2-ol 
• 63315-69-5 (-)-(4R)-4-hydroxypentan-2-one 
• 22520-29-2 syn-3,4-epoxy-2-pentanol 
• 64-17-5 ethanol 
• 60-29-7 diethyl ether 
• 7732-18-5 water 
• 7664-93-9 sulfuric acid 
• 56-81-5 glycerol 
• 930-18-7 cis-1,2-dimethylcyclopropane 
• 7570-05-0 cis-4,6-dimethyl-2-oxo-1,3-dioxane 
• 73836-68-7 (S)-4-hydroxypentan-2-one 
• 111957-98-3 Pent-4-en-2-ol 

Downstream Products

• 94309-72-5 2,4-bis-phenylcarbamoyloxy-pentane 
• 504-60-9 penta-1,3-diene 
• 19398-53-9 2,4-dibromopentane 
• 101421-04-9 nitric acid-(1,3-dimethyl-propanediyl ester) 
• 107-87-9 2-Pentanone 
• 35196-66-8 syn-pentane-2,4-diyl bis(4-methylbenzenesulfonate) 
• 74012-33-2 2-[4-(4c,6c-dimethyl-[1,3]dioxan-2r-yl)-phenyl]-4,4-dimethyl-4,5-dihydro-oxazole 
• 74012-33-2 2-[4-(4r,6t-dimethyl-[1,3]dioxan-2-yl)-phenyl]-4,4-dimethyl-4,5-dihydro-oxazole 
• 71671-14-2 C₁₉H₃₁NO₄ 
• 42075-35-4 4-(4r,6t-dimethyl-[1,3,2]dioxaborinan-2-yl)-benzoic acid 
• 7317-42-2 2,4-pentanediol phenylboronic ester 
• 34322-81-1 2-Phenoxy-4,6-dimethyl-1,3,2-dioxaborinan 
• 4727-93-9 4,6-dimethyltrimethylene (cis,cis) sulphite 
• 89238-89-1 (4R,6R)-4,6-Dimethyl-2-(4-nitro-phenyl)-[1,3]dioxane 

Relevant academic research and scientific papers

Efficient separation of diastereomeric mixtures of syn - And anti -2,4-pentanediol

A simple and practical process was developed for the efficient separation of diastereomeric syn- and anti-2,4-pentanediol by selective acetalization of a diastereomeric mixture of the 2,4-pentanediols and selective hydrolysis of the corresponding acetals. The process relies upon the reaction rate differences of syn-2,4-pentanediol (syn-diol) and anti 2,4-pentanediol (anti-diol) in acetalization and of the corresponding acetals in hydrolysis: the syn-diol reacts faster to form a more stable acetal than the anti-diol, which in turn is more susceptible to hydrolysis by Bronsted acid. Acetalization of a 2,4-pentanediol diastereomeric mixture (syn/anti = 45:55) with acetophenone (0.95 equiv relative to syn-diol) leads to the formation of a syn-enriched acetal mixture with a syn/anti diastereomeric ratio (drs/a) of 6:1, leaving an anti-enriched diol mixture (drs/a = 1:7). Subsequent kinetic resolution via selective hydrolysis of the minor anti-acetal with a catalytic amount of 1.0 N HCl at ambient temperature affords the pure syn-acetal (drs/a > 99:1) in the organic phase and the anti-enriched 2,4-pentanediols (drs/a = 1:6) in the aqueous phase, which are conveniently separated by a phase cut. Hydrolysis of the syn-acetal is facile in alcohol solvents at elevated temperatures (60-80 °C), yielding the pure syn-diol. A second acetalization of the anti-enriched 2,4-pentanediols leads to the pure anti-2,4-pentanediol. This separation gives the syn-diol in 75-79% yield with drs/a > 99:1 and the anti-diol in 79-85% yield with dra/s > 98:2. Additionally, the acetophenone used for the acetalization can be recovered in 88-92% yield, and therefore, the overall process is high-yielding, atom-economical, and potentially recyclable.

The Stereo-differentiating (Asymmetric) Hydrogenation of the C=O Double Bond with a Modified Nickel Catalyst.XXXV. A Facile Method for the Preparation of Oplically Pure β-Diols

The hydrogenation of RCOCH2COR over a Raney nickel catalyst modified with a mixture of tartaric acid and NaBr gave (R*,R*)-RCH(OH)CH2CH(OH)R selectively with a high optical purity.The substrates with R=CH3-,CH3CH2-, CH3CH2CH2-, CH3(CH2)4CH2-, and Ph- were employed in this study.In all cases, the recrystallization of the hydrogenation product gave an optically pure (R*,R*)-isomer which was free from the (R*,S*)-isomer.

Stereoselective generation of 1,3- and 1,4-dioxy-substituted carbanions by sparteine-assisted deprotonation of chiral precursors: Substrate or reagent control in the synthesis of α, γ- and α,δ-diols

The deprotonation of a dicarbamate, derived from (S)-butane-1,3-diol, by sec-butyllithium takes an highly diastereoselective, but opposite, direction in the presence of (-)-sparteine and of tetramethylethylenediamine (TMEDA), respectively. The (S)-pentane-1,4-diol derivative shows the same stereochemical preference under both conditions.

n-Alkyl glycosides and p-hydroxybenzoyloxy glucose from fruits of Crescentia cujete

The fruits of Crescentia cujete afforded eight new compounds, along with four known compounds, acanthoside D, β-D-glucopyransoyl benzoate, (R)-1-O-β-D-glucopyranosyl-1,3-octanediol, and β-D-fructofuranosyl 6-O-(p-hydroxybenzoyl)-α-D-glucopyranoside. The structures of the new glycosides were established as three glycosides of (2R,4S)-2,4-pentanediol, two glycosides of (R)-4-hydroxy-2-pentanone, two glycosides of (R)-1,3-octanediol and 6-O-(p-hydroybenzoyl)-D-glucose, by spectroscopic and chemical methods.

Stereoselective methoxyselenenylation of acyclic allylic alcohol derivatives: A method for the synthesis of 1,3-anti-diols

Reaction of secondary acyclic trans-allylic alcohol derivatives with PhSeBr in the presence of 2,6-di-t-butylpyridine in MeOH proceeded in a highly regio- and stereoselective manner and the subsequent reduction and deprotection of the resultant methoxyselenides afforded mostly 1,3-anti-diols. The methoxyselenenylation of the acetate derivative of the same allylic alcohol, on the other hand, gave several other isomers along with the 1,3-anti-diol derivative.

The chemistry of tetrachlorodiborane(4). II. Reactions with saturated ring hydrocarbons

Tetrachlorodiborane(4) reacts with cyclopropane, methylcyclopropane and dimethylcyclopropanes to give ring cleavage addition compounds. IR and NMR data support structures with dichloroboryl groups in the 1,3 position of the hydrocarbon chain. Some evidence is presented to support a stereospecific reaction which involves a 4-centered transition state comparable to that which has been postulated for subchloride addition to olefins. No reaction occurs with 1,1-dichlorocyclopropane or cyclobutane.

Chemoselective formation of cyclo-aliphatic and cyclo-olefinic 1,3-diolsviapressure hydrogenation of potentially biobased platform molecules using Kn?lker-type catalysts

The hydrogenative conversions of the biobased platform molecules 4-hydroxycyclopent-2-enone and cyclopentane-1,3-dione to their corresponding 1,3-diols are established using a pre-activated Kn?lker-type iron catalyst. The catalyst exhibits a high selectivity for ketone reduction, and does not induce dehydration. Moreover, by using different substituents of the ligand, thecis-transratio of the products can be affected substantially. A decent compatibility of this catalytic system with various structurally related substrates is demonstrated.

Synthesis and Applications of (Pyridyl)imine Fe(II) Complexes as Catalysts in Transfer Hydrogenation of Ketones

Abstract: Chiral (pyridyl)imine Fe(II) complexes, [Fe(L1)3]2+[PF6?]2, (Fe1), [Fe(L2)3]2+[PF6?]2, (Fe2), [Fe(L3)3]2+[PF6?]2 (Fe3), and [Fe(L4)3]2+[PF6?]2 (Fe4) were synthesised by reactions of synthons (S-)-1-phenyl-N-(pyridine-2-yl) ethylidine)ethanamine (L1), (R-)-1-phenyl-N-(pyridine-2-yl) ethylidine) ethanamine (L2), (S)-1-phenyl-N-(pyridine-2-yl methylene) ethanamine (L3) and (S)-1-phenyl-N-(pyridine-2-yl methylene)ethanamine (L4) with the FeCl2 salt. The solid-state structure of complex Fe4 showed that the?Fe atom contains three units of bidentate bound ligand L4 to form a six-coordinate cationic compound. The Fe(II) complexes were evaluated as catalysts in asymmetric transfer hydrogenation of ketones reactions and showed moderate catalytic activities with low enantioselectivity. Catalytic activities of the respective complexes were regulated by the nature of the metal complexes, ketone substrate and reaction conditions. Mercury and sub-stoichiometric poisoning experiments implicate possible formation of both active Fe(0) nanoparticles and Fe(II) homogeneous intermediates. Graphic Abstract: [Figure not available: see fulltext.]

Method for preparing beta-diol from beta-diketone

The invention relates to a method for preparing beta-diol from beta-diketone. The method is characterized in that beta-diketone contacts and reacts with hydrogen in the presence of a hydrogenation catalyst under fixed bed reaction conditions, the hydrogenation catalyst comprises an active component copper and a carrier, and the hydrogenation catalyst preferably comprises an assistant component selected from VIIIB and IB group elements, the assistant is preferably selected from one or more of Ni, Co and Ag, and the carrier is SiO2. The method adopting a fixed bed hydrogenation technology and using a copper-containing supported catalyst has the advantages of no pollution to environment, mild operating conditions, and suitableness for continuous production.

Method for preparing beta-diol from beta-diketone by hydrogenation

The invention relates to a method for preparing beta-diol from beta-diketone by hydrogenation. The method comprises the following steps: in the presence of a catalyst and under the fixed-bed hydrotreating reaction condition, enabling beta-diketone to be in contact with hydrogen, so as to obtain beta-diol, wherein the catalyst contains CuO and ZnO, preferably also contains Al2O3, and more preferably also contains alkali metal oxides. According to the method for preparing beta-diol from beta-diketone by hydrogenation, provided by the invention, the technology of continuously producing beta-diol by adopting a fixed bed device is realized, the technology is simple and convenient to operate, the utilization ratio of raw materials and the production efficiency of products are improved, the reaction does not need to be carried out under high pressure, and potential safety hazards are reduced.