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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324929생성일: 2026년 10월 24일

Hydrochloric Acid → 16-Mercaptohexadecanoic acid

https://huagongshe.com/ko/reaction/324929

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물2-Thiopheneacetic acidHCID 15970—
반응물16-Bromohexadecanoic acidHCID 620397—
반응물SodiumHCID 5360545—
용매MethanolHCID 887—
생성물16-Mercaptohexadecanoic acidHCID 352258597.2%

반응 단계

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 recrystalization from n-hexane, filtering out and drying over high vacuum. 5.1 gr (97% yield) of the desired product were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06221583B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-d5bc83519e80436ba7173273d3b8b69a
출처 메모uspto-grants-2001_04