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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111554Generated: October 28, 2026

Stearoyl chloride → HCID 15095407, compound

https://huagongshe.com/reaction/1111554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStearoyl chlorideHCID 8212—
ReactantTriethylamineHCID 8471—
Reactant2-Nitrobenzyl alcoholHCID 11923—
SolventBenzeneHCID 241—
ProductHCID 15095407HCID 15095407—

Reaction Steps

In 100 ml benzene were mixed 2-nitrobenzyl alcohol (7.65 g, 0.05 mol) and triethylamine (5.06 g, 0.05 mol). To the solution octadecanoyl chloride (15.14 g, 0.05 mol) was added dropwise with stirring. The mixture was stirred an additional one hour and the precipitated triethyl amine hydrochloride was removed by filtration. The filtrate was evaporated to dryness and the residue crystallized from ethanol (yield 13.0 g, m.p. 60°-61° C.). The tetradecanoate (m.p. 46° C.) (Compound 5), hexadecanoate (m.p. 54° C.) (Compound 6), heptadecanoate (m.p. 48° C.) (Compound 7), and 9-octadecenoate (Compound 8) esters of 2-nitrobenzyl alcohol were similarly prepared using corresponding acyl chlorides in place of octadecanoyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980096
Source datasetuspto-grants-1990_12
ORD IDord-b62e655f84954ceeb707324376b49c77
Source noteuspto-grants-1990_12