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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1168881생성일: 2026년 10월 27일

Boron Trichloride → 2,2,2-trifluoro-N-(7-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-N-propyl-acetamide

https://huagongshe.com/reaction/1168881

반응식

참여 물질

역할이름HCID투입량
반응물Boron TrichlorideHCID 25135—
반응물2,2,2-trifluoro-N-(7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-N-propyl-acetamideHCID 22560679—
촉매Tetrabutylammonium IodideHCID 67553—
용매DichloromethaneHCID 6344—
생성물2,2,2-trifluoro-N-(7-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-N-propyl-acetamideHCID 2256066094.4%

반응 단계

To a −78° C. solution of 2,2,2-trifluoro-N-(7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-N-propyl-acetamide (3.4 g, 10.9 mmol) and tetrabutylammonium iodide (4.43 g, 12.0 mmol) in dichloromethane (200 mL) under an inert atmosphere boron trichloride (1 M, 27.2 mL) was added dropwise. The reaction was warmed to room temperature and stirred for 2.5 h. The reaction was quenched by the slow addition of water. The organic layer was separated and dried (MgSO4). This was concentrated onto silica (15 g) and placed on top of a flash column. Chromatography eluting with 30% acetone in hexanes afforded 2,2,2-trifluoro-N-(7-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-N-propyl-acetamide as a foam (3.1 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06627644B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-be972d537b8f4704b4f5f4e5bcfc4d7c
출처 메모uspto-grants-2003_09