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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371008생성일: 2026년 10월 25일

Acetaldehyde → 6,7-Dichloro-5-hydroxy-alpha-methylbenzo[b]thiophene-2-methanol

https://huagongshe.com/reaction/371008

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물Hydrochloric AcidHCID 313—
반응물6,7-Dichloro-1-benzothiophene-5-olHCID 13289997—
반응물Carbontetrachloride dry-iceHCID 86602444—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물6,7-Dichloro-5-hydroxy-alpha-methylbenzo[b]thiophene-2-methanolHCID 13477654—

반응 단계

To a solution of 25 g of 6,7-dichloro-5-hydroxybenzo[b]thiophene in 145 ml of dried tetrahydrofuran at -25° to -30° is added 110 ml of 2.5M n-butyllithium maintaining a temperature below -21°. After the addition, the carbon tetrachloride-dry ice bath is replaced with an ice-water bath and the mixture is stirred at 0°-5° for 4 hrs. A solution of 7.5 ml of freshly distilled acetaldehyde in 10 ml tetrahydrofuran is added dropwise. And additional 2 ml of acetaldehyde is added and the solution is stirred for 1 hr. The solution is poured onto 500 ml of a cold 5% hydrochloric acid solution and the mixture is extracted with ethyl ether. The ether extracts are washed, dried over anhydrous magnesium sulfate, filtered and solvent is removed to give a solid. Recrystallization from ethyl acetate and hexane gives 20 g of 6,7-dichloro-5-hydroxy-α-methylbenzo[b]thiophene-2-methanol, mp 173°-174°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04528399
출처 데이터셋uspto-grants-1985_07
ORD IDord-be3fe63115264d5db3c89544b72c8512
출처 메모uspto-grants-1985_07