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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633187Generated: November 1, 2026

Stearoyl chloride → HCID 70359046, compound

https://huagongshe.com/reaction/1633187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStearoyl chlorideHCID 8212—
ReactantBenzoinHCID 8400—
ReactantHCID 4622696HCID 4622696—
ReactantPerfluorooctanoateHCID 4986139—
ReactantHCID 9991962HCID 9991962—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
ProductHCID 70359046HCID 70359046—

Reaction Steps

3'-Methoxybenzoin (5 g, 0.021 mol) was dissolved in 200 ml of toluene containing one equivalent of triethylamine. One equivalent of octadecanoyl chloride in 20 ml of toluene was added slowly to the cooled (ice bath) stirred benzoin solution. Stirring was continued with ice bath cooling for one hour. The reaction mixture was then filtered free of precipitated amine salt and the filtrate was evaporated to give an oil which solidified to give a low melting solid. The hexadecanesulfonate (Compound 14) and perfluorooctanoate (Compound 15) (m.p. 55°-58° C.) esters were similarly prepared from the corresponding acid chlorides.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04478967
Source datasetuspto-grants-1984_10
ORD IDord-1cd44c9feff044bd8d8b787a575d2e93
Source noteuspto-grants-1984_10