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Merck
CN

477907

Sigma-Aldrich

碳酸二苄酯

99%

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关于此项目

线性分子式:
(C6H5CH2O)2CO
化学文摘社编号:
分子量:
242.27
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案

99%

沸点

180-190 °C/2 mmHg (lit.)

mp

29-33 °C (lit.)

SMILES字符串

O=C(OCc1ccccc1)OCc2ccccc2

InChI

1S/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

InChI key

PIZLBWGMERQCOC-UHFFFAOYSA-N

一般描述

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.

应用

Dibenzyl carbonate may be used in the synthesis of the following via benzylation reaction:
  • Benzyl phenyl ether from phenol.
  • 2,3-Diphenylpropionitrile from phenylacetonitrile.
  • Benzyl 2,3-diphenylpropionate from benzyl phenyl acetate.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

Lot/Batch Number

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Synthesis of dibenzyl carbonate: towards a sustainable catalytic approach.
Fiorani G and Selva M.
Royal Society of Chemistry Advances, 4(4), 1929-1937 (2014)
Selective mono-benzylation of methylene active compounds with dibenzyl carbonate: benzylation of phenol.
AlbertoaMarques C.
Journal of the Chemical Society. Perkin Transactions 1, 15, 1889-1893 (1995)
Selective N,N-dibenzylation of primary aliphatic amines with dibenzyl carbonate in the presence of phosphonium salts.
Loris A, et al.
The Journal of Organic Chemistry, 69(11), 3953-3956 (2004)

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