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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745712Generated: October 31, 2026

Stearoyl chloride → HCID 15095407, compound

https://huagongshe.com/reaction/745712

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 numberUS04599273
Source datasetuspto-grants-1986_07
ORD IDord-0c95190a4287431291d2c4650008ec3e
Source noteuspto-grants-1986_07