Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372205Generated: October 31, 2026

Oxalyl chloride → HCID 21069967, compound

https://huagongshe.com/reaction/1372205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 21069793HCID 21069793—
SolventMethanolHCID 887—
ProductHCID 21069967HCID 2106996796%

Reaction Steps

Reaction of intermediate 9, 2-(2-(methylthio)ethoxy)propanoic acid, (13.70 g, 0.083 mol) with oxalyl chloride followed by reaction with methanol gave 14.27 g (96% yield) of the title ester as a clear oil; bp 55–60° C./0.3 torr (bulb to bulb distillation, air bath temperature). 1HNMR 400 MHz (CDCl3) δ ppm: 1.42 (3H, d, J=7.0 Hz, CH3), 2.15 (3H, s, SCH3), 2.71 (2H, t, J=6.8 Hz, CH2), 3.56 (1H, m, CH), 3.75 (3H, s, OCH3), 3.78 (1H, m, CH), 4.15 (1H, q, J=7.0 Hz, OCH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157447B2
Source datasetuspto-grants-2007_01
ORD IDord-041bdc13666a4552b946fd03dd212cad
Source noteuspto-grants-2007_01