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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1450436생성일: 2026년 10월 25일

Triethylamine → [Benzo[b]thiophene-2-yl][1-(2-phenylethyl)-4-piperidinyl]methanone

https://huagongshe.com/reaction/1450436

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물alpha-[1-(2-Phenylethyl)-4-piperidinyl]-2-benzo[b]thiophenemethanolHCID 18930341—
용매Dimethyl SulfoxideHCID 679—
용매DichloromethaneHCID 6344—
생성물[Benzo[b]thiophene-2-yl][1-(2-phenylethyl)-4-piperidinyl]methanoneHCID 18930331—

반응 조건

온도-78 °C

반응 단계

Dissolve oxalyl chloride (4.22 g, 33.28 mmol) in methylene chloride (200 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, dimethylsulfoxide (5.42 g, 69.33 mmol) and stir at -78° C. for 15 minutes. Add, by dropwise addition, a solution of α-[1-(2-phenylethyl)-4-piperidinyl]-2-benzo[b]thiophenemethanol in dimethylsulfoxide (150 mL). Stir at -78° C. for 30 minutes, add triethylamine (15.18 g, 0.150 mol) and stir at -78° C. for 1 hour. Remove the ice bath and stir for an additional 1.5 hours. Evaporate the solvent in vacuo and recrystallize (isopropanol) to give the title compound as a fluffy white crystalline solid; mp 129°-130° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05602147
출처 데이터셋uspto-grants-1997_02
ORD IDord-ab9e7411503545679f9b56bfd49fdf54
출처 메모uspto-grants-1997_02