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3459-92-5

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3459-92-5 Usage

Chemical Properties

Colorless low melting solid

Uses

Ionic liquids can effectively accelerate slow N-benzylation reactions utilizing dibenzyl carbonate as an alkylating reagent. Dibenzyl carbonate (DBzlC) has been used to benzylate phenylacetonitrile, benzyl phenylacetate and phenol. Selective N, N-dibenzylation of primary aliphatic amines was carried with dibenzyl carbonate in the presence of phosphonium salts.

Preparation

To a stirred solution of benzyl alcohol (0.216 g, 2.00 mol), tributylphosphine (0.303 g, 1.50 mmol), and CyTMG (0.394 g, 2.00 mmol) in DMF (2.00 mL), CO2 was added at room temperature. After 15 min, tetrabromomethane (0.663 g, 2.00 mmol) was added, the reaction vessel was sealed, and the contents were stirred for 2 h. Thereafter, the reaction mixture was diluted with ethyl acetate, washed successively with 0.5 m aqueous HCl and saturated aq. NaHCO3 solution, and dried over Na2SO4. Diphenylmetha- nol was added to the organic solution as an internal standard and the yield of dibenzyl carbonate was determined from the relative integrals of a methylene peak of the carbonate and a methine peak of diphenylmethanol in the 1H NMR spectrum of the ethyl acetate solution. Dibenzyl carbonate, prepared by a larger scale reaction of CO2 with benzyl alcohol (1.08 g, 10.0 mmol), was isolated by column chromatography (cyclohexane/ethyl acetate, 50:1) in 67.3% yield (0.816 g).

General Description

Dibenzyl carbonate (DBC) is commonly used as a benzylating agent. Dimethyl carbonate and excess of benzyl alcohol undergoes transesterification in the presence of CsF/α-Al2O3 (cesium fluoride/aluminum oxide) to form DBC. The formation of N,N-dibenzyl derivatives by the reaction of primary aliphatic amines with DBC in the presence of phosphonium salts has been investigated.

Check Digit Verification of cas no

The CAS Registry Mumber 3459-92-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3459-92:
(6*3)+(5*4)+(4*5)+(3*9)+(2*9)+(1*2)=105
105 % 10 = 5
So 3459-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O3/c16-15(17-11-13-7-3-1-4-8-13)18-12-14-9-5-2-6-10-14/h1-10H,11-12H2

3459-92-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (C1600)  Dibenzyl Carbonate  >98.0%(GC)

  • 3459-92-5

  • 1g

  • 235.00CNY

  • Detail
  • TCI America

  • (C1600)  Dibenzyl Carbonate  >98.0%(GC)

  • 3459-92-5

  • 5g

  • 660.00CNY

  • Detail
  • Alfa Aesar

  • (A11464)  Dibenzyl carbonate, 98%   

  • 3459-92-5

  • 10g

  • 764.0CNY

  • Detail
  • Alfa Aesar

  • (A11464)  Dibenzyl carbonate, 98%   

  • 3459-92-5

  • 50g

  • 3056.0CNY

  • Detail
  • Alfa Aesar

  • (A11464)  Dibenzyl carbonate, 98%   

  • 3459-92-5

  • 250g

  • 11299.0CNY

  • Detail
  • Aldrich

  • (477907)  Dibenzylcarbonate  99%

  • 3459-92-5

  • 477907-5G

  • 739.44CNY

  • Detail

3459-92-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name DIBENZYL CARBONATE

1.2 Other means of identification

Product number -
Other names Carbonic acid,bis(phenylmethyl) ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3459-92-5 SDS

3459-92-5Relevant articles and documents

Direct Synthesis of Alkyl 2-Alkynoates from Alk-1-ynes, CO2, and Bromoalkanes Catalysed by Copper(I) or Silver(I) Salt

Fukue, Yasuo,Oi, Shuichi,Inoue, Yoshio

, p. 2091 - 2092 (1994)

Alkyl alkynoates are synthesized directly from alk-1-ynes, CO2, and bromoalkanes in the presence of a catalytic amount of copper(I) or silver(I) salt.

METHOD OF CONVERTING CARBON DIOXIDE INTO CARBONYL COMPOUNDS

-

Page/Page column 15; 16, (2019/05/02)

The present invention provides a method for fixing carbon dioxide gas as a carbonyl compound represented by formula (3) as depicted by Figure 1 and comprising, purging of carbon dioxide in a solution of a nucleophile represented by the formula (1) in presence of a solvent at a temperature ranging from -40 Degree Celsius to 35 Degree Celsius, followed by adding a reagent at temperature ranging from -40 degree to 35 degree and thereafter adding another nucleophile represented by the formula (2) to obtain carbonyl compound represented by formula (3). The present invention can be advantageously used to obtain commercially important carbonyl compounds and clean unwanted carbon dioxide gas from the atmosphere and industrial effluents.

Carbon Dioxide Utilisation for the Synthesis of Unsymmetrical Dialkyl and Cyclic Carbonates Promoted by Basic Ionic Liquids

Goodrich, Peter,Gunaratne, H. Q. Nimal,Jin, Lili,Lei, Yuntao,Seddon, Kenneth R.

, p. 181 - 185 (2018/03/09)

An efficient and greener synthesis of unsymmetrical organic carbonates mediated by Hünig's base-appended basic ionic liquids, via carbon dioxide conversion, is described here. These ionic liquids were found to be effective bases for the fixation of carbon dioxide by various alcohols and benzyl bromide, at room temperature. When the alcohol and the halide functionalities are present within the same substrate, the reaction cleanly produces a cyclic carbonate. These functionalised basic ionic liquids were fully recyclable with no loss product yields.

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