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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131072Generated: October 25, 2026

Hydrochloric Acid → 16-Mercaptohexadecanoic acid

https://huagongshe.com/reaction/131072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-Thiopheneacetic acidHCID 15970—
Reactant16-Bromohexadecanoic acidHCID 620397—
ReactantSodiumHCID 5360545—
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 thiolacetic 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 recrystallization from n-hexane, filtering out and drying over high vacuum. 5.1 gr (97% yield) of the desired product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384749B2
Source datasetuspto-grants-2008_06
ORD IDord-5d15ca3632604c9695ee40e56f73019e
Source noteuspto-grants-2008_06