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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1479156생성일: 2026년 10월 26일

Triethylamine → 2,6-difluoro-N-formyl-N-vinyl-benzamide

https://huagongshe.com/reaction/1479156

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-Butyl methyl etherHCID 15413—
반응물N-VinylformamideHCID 83191—
반응물2,6-Difluorobenzoyl chlorideHCID 87438—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2,6-difluoro-N-formyl-N-vinyl-benzamideHCID 8976076987%

반응 단계

2,6-difluorobenzoyl chloride (35.4 ml, 50 g, 284 mmol) was added dropwise with stirring to a solution of N-vinylformamide (18 ml, 18.3 g, 258 mmol), 4-dimethylaminopyridine (3.1 g, 25.8 mmol), and triethylamine (53.8 ml, 39 g, 387 mmol) in dichloromethane (200 ml). The temperature was kept at ca 20° C. with an ice/water bath. After the addition the mixture was stirred two hours at room temperature then shaken between tBuOMe and water. The organic phase was washed with half saturated brine, dried with Na2SO4 and evaporated to give 47 g (87% crude) of 2,6-difluoro-N-formyl-N-vinyl-benzamide, which contained ca 60% of 2,6-difluoro-N-vinyl-benzamide, which is the product of the next step, in which the formyl group has already been cleaved.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09408392B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-3c297fe837944e6ba6e9cec933846fa3
출처 메모uspto-grants-2016_08