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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501348생성일: 2026년 10월 25일

Sodium Hydroxide → 1-[2-[4-(6-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperazin-1-yl]-ethyl]-cyclopropanecarboxylic acid tert-butyl ester

https://huagongshe.com/reaction/501348

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-(6-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperazineHCID 11289155—
반응물Tert-Butyl 1-(2-oxoethyl)cyclopropanecarboxylateHCID 58817571—
용매DichloromethaneHCID 6344—
생성물1-[2-[4-(6-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperazin-1-yl]-ethyl]-cyclopropanecarboxylic acid tert-butyl esterHCID 5881761591.2%

반응 단계

To a solution of 4.2 g (14.7 mmol) of 1-(6-trifluoromethyl-benzo[b]thiophen-3-yl)-piperazine in 100 mL of dichloromethane under nitrogen was added 3.5 g (19.1 mmol) of 1-(2-Oxo-ethyl)-cyclopropanecarboxylic acid tert-butyl ester. After stirring 10 minutes at room temperature 6.5 g (30.7 mmol) of sodium triacetoxyborohydride was added portion-wise. After 30 minutes 100 mL of 0.5 N aqueous sodium hydroxide was added and the reaction was stirred for 15 minutes. The organic layer was separated, dried and concentrated to deliver a paste. This was taken up in methanolic hydrogen chloride. The salt thus obtained was recrystallized from ethyl acetate/methanol to deliver 6.6 g (13.4 mmol) of the desired product as a white powder mp=187-9° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772252B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-37dd843dc371497e923b2aafdc91a92c
출처 메모uspto-grants-2010_08