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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477093Generated: October 30, 2026

Oxalyl chloride → HCID 90411212, compound

https://huagongshe.com/reaction/1477093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant(2E)-2-Tetradecenoic acidHCID 5282738—
SolventDichloromethaneHCID 6344—
ProductHCID 90411212HCID 9041121299%

Reaction Steps

(E)-tetradec-2-enoic acid (18.7 g) was dissolved in anhydrous dichloromethane (200 ml) under nitrogen with stirring. The solution was cooled in ice-water bath for 30 min. Oxalyl chloride (9.1 ml) was added dropwise. The reaction mixture was slowly warm up to room temperature overnight. The solvent was removed under vacuum. The product was obtained as clear oil (20.0 g, 99%) and used in next step synthesis without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403760B2
Source datasetuspto-grants-2016_08
ORD IDord-71886ac2884f47f98bee611e78b160d8
Source noteuspto-grants-2016_08