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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1267622생성일: 2026년 10월 26일

Hydrochloric Acid → 3',4',5'-Trimethoxycinnamyl alcohol

https://huagongshe.com/reaction/1267622

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물3-(3,4,5-Trimethoxyphenyl)acrylic acidHCID 7021—
반응물Ethyl chloroformateHCID 10928—
반응물Sodium borohydrideHCID 4311764—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물3',4',5'-Trimethoxycinnamyl alcoholHCID 73924—

반응 단계

3,4,5-Trimethoxycinnamic acid (1.5 g) was dissolved in THF (100 mL), triethylamine (0.64 mL) was added to the solution under ice cooling, and ethyl chlorocarbonate (0.44 mL) was then added dropwise thereto. After stirring the resultant mixture at room temperature for 1 hour, sodium borohydride (477 mg) was added to the mixture under ice cooling. After stirring the resultant mixture at room temperature for 1 hour, diluted hydrochloric acid was added to the reaction mixture to conduct extraction with chloroform. The resultant organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1) to obtain the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06552188B2
출처 데이터셋uspto-grants-2003_04
ORD IDord-b1259147d3e147f487dc04a96e5576dc
출처 메모uspto-grants-2003_04