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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107667Generated: October 30, 2026

Hydrochloric Acid → 16-Mercaptohexadecanoic acid

https://huagongshe.com/reaction/1107667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant16-Bromohexadecanoic acidHCID 620397—
ReactantSodiumHCID 5360545—
ReactantHCID 178418634HCID 178418634—
SolventMethanolHCID 887—
Product16-Mercaptohexadecanoic acidHCID 352258597.2%

Reaction Steps

Under inert atmosphere 2.0 gr of sodium metal suspension (40% in mineral oil) were slowly added to 100 ml of dry methanol at 0° C. At the end of the addition reaction mixture was stirred for 10 min at RT and 1.75 ml (21.58 mmole) of thioacetic acid were added. After additional 10 min of stirring, 30 ml degassed methanolic solution of 6.1 gr (18.19 mmole) of 16-bromohexadecanoic acid were added. The resulted mixture was refluxed for 15 hrs, after which, allowed to cool to RT and 50 ml of degassed 1.0 M NaOH aqueous solution were injected. Additional refluxing for 3 hrs required for reaction completion. 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 removal of ether material was purified by recrystalization from n-hexane, filtering out and drying over high vacuum. 5.1 gr (97% yield) of the desired product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063573
Source datasetuspto-grants-2000_05
ORD IDord-262bcc7c01d74baebb47d4c9aa9a4b23
Source noteuspto-grants-2000_05