反应 #1265352

ord-3c560266ba7246c3813e8b3a210bf2fe

反应方程式

Cc1ccccc1
toluene
O=C(Cl)C(=O)Cl
Oxalyl chloride
COCCOCCOCCOCC(=O)O
{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-acetic acid
COCCOCCOCCCOCC(=O)Cl
CH3(OCH2CH2)3CH2OCH2COCl
收率 99.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他(CH3(OCH2CH2)3CH2OCH2COCl) was prepared

实验过程

(CH3(OCH2CH2)3CH2OCH2COCl) was prepared according to Procedure 1. Oxalyl chloride (3.6 mL, 0.041 mol); {2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-acetic acid (3.3 g, 0.15 mol); pyridine (0.1 mL, 1 mmol) and anhydrous toluene (10 mL) to give CH3(OCH2CH2)3CH2OCH2COCl as yellow oil (3.5 g, 99%). This compound was used without any further purification.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07276286B2uspto-grants-2007_10