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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130290Generated: October 26, 2026

Hydrochloric Acid → 16-Sulfanylhexadecan-1-ol

https://huagongshe.com/reaction/130290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-Thiopheneacetic acidHCID 15970—
Reactant16-Bromo-1-hexadecanolHCID 2757013—
ReactantSodiumHCID 5360545—
SolventMethanolHCID 887—
Product16-Sulfanylhexadecan-1-olHCID 376324670.3%

Reaction Steps

Under inert atmosphere 365 mg of sodium metal suspension (40% in mineral oil) were added dropwise to 20 ml of dry methanol at 0° C. After completion of addition the reaction mixture was stirred for 10 min at RT followed by addition of 0.45 ml (6.30 mmole) of thiolacetic acid. After additional 10 min of stirring 3 ml degassed methanolic solution of 1.0 gr (3.11 mmole) of 16-bromohexadecan-1-ol were added. The resulted mixture was refluxed for 15 hrs, allowed to cool to RT and 20 ml of degassed 1.0 M NaOH aqueous solution were injected. The reaction completion required additional 3 hr of reflux. Resulted reaction mixture was cooled with ice bath and poured, with stirring, into a vessel containing 200 ml of ice water. This mixture was titrated to pH=7 by 1.0 M HCl and extracted with 300 ml of ether. The organic layer was separated, washed with 3×150 ml of water, 150 ml of saturated NaCl aqueous solution and dried over sodium sulfate. After ether removal material was dissolved in minimum amount of dicloromethane and purified by silica gel chromatography (100% dicloromethane as eluent). 600 mg (70% yield) of the desired product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381533B2
Source datasetuspto-grants-2008_06
ORD IDord-cff93c7315334c5b974b677153d14cdb
Source noteuspto-grants-2008_06