acetyl isopropyl carbonate

Base Information

Chemical Name:acetyl isopropyl carbonate
CAS No.:60059-18-9
Molecular Formula:C₆H₁₀O₄
Molecular Weight:146.143
Hs Code.:

Synonyms:acetyl isopropyl carbonate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of acetyl isopropyl carbonate

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Technology Process of acetyl isopropyl carbonate

There total 1 articles about acetyl isopropyl carbonate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 36.0%

: 25424-50-4
acetyl 2-methylpropionyl peroxide

: 108-21-4
Isopropyl acetate

: 60059-18-9
acetyl isopropyl carbonate

: 64-19-7,77671-22-8
acetic acid

Guidance literature:: In tetrachloromethane; at 50 ℃; Kinetics; Product distribution; Thermodynamic data; E_a values, other solvents, other temperatures;

Reference yield: 97.0%

: 93-54-9
1-Phenyl-1-propanol

: 60059-18-9
acetyl isopropyl carbonate

: 2114-29-6,83808-03-1,83860-48-4,84275-44-5
(R)-1-phenylpropyl acetate

Guidance literature:: With (-)-(C₅Ph₅)FeC₅H₃NC₃H(dimethylamino); dicarbonyl(chloro)(η⁵-pentaphenylcyclopentadienyl)ruthenium(II); potassium tert-butylate; In tert-Amyl alcohol; toluene; at 10 ℃; for 48h; enantioselective reaction; Inert atmosphere; Resolution of racemate;
DOI:10.1021/ja307425g

Reference yield: 97.0%

: 60059-18-9
acetyl isopropyl carbonate

: 1006037-12-2
methyl 4-(1-azidoethyl)benzonitrile

: N-(1-(4-cyanophenyl)ethylidene)acetamide

Guidance literature:: With ([2,5-Me2-3,4-Ph2(η5-C4CNHPh)]Ru(CO)(μ-CO))2; In tetrahydrofuran; at 20 ℃; for 3h; chemoselective reaction; Irradiation; Inert atmosphere; Schlenk technique;
DOI:10.1002/adsc.201601406