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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20519생성일: 2026년 10월 24일

Triethylamine → 1-(3,4-Difluorobenzoyl)azetidine

https://huagongshe.com/ko/reaction/20519

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물3,4-Difluorobenzoic acidHCID 99166—
반응물Azetidine hydrochlorideHCID 12308726—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물1-(3,4-Difluorobenzoyl)azetidineHCID 5934685950.7%

반응 단계

Oxalyl chloride (1.05 mL, 12.0 mmol) was added to a solution of 3,4-difluorobenzoic acid (1.58 g, 10 mmol) in DCM (50 mL) containing DMF (1 drop). The reaction was stirred at ambient temperature for 16 h then evaporated to dryness. The residue was redissolved in DCM (25 mL) and azetidine hydrochloride (1.12 g, 12.0 mmol) added followed by triethylamine (4.18 mL, 30.0 mmol). The mixture was stirred at ambient temperature for 2 h then concentrated in vacuo. The residue was partitioned between ethyl acetate and 1N hydrochloric acid, the organic phase washed with a saturated aqueous solution of sodium bicarbonate followed by brine, dried (MgSO4), and concentrated in vacuo. The title compound was crystallized from an ethyl acetate/hexane mixture to give a white crystalline solid (1.0 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745475B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-35f62b13bbf54e95be508ca62a2d14d2
출처 메모uspto-grants-2010_06