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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 657555생성일: 2026년 10월 25일

Triethylamine → 3-Acryloyl-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/657555

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Acryloyl chlorideHCID 13140—
반응물7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochlorideHCID 22004098—
용매DichloromethaneHCID 6344—
생성물3-Acryloyl-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 68532781—

반응 조건

온도0 °C

반응 단계

At ambient temperature, 70 g (287.2 mmol) of the product obtained in Step 2 are dissolved in 1200 mL of dichloromethane, and then 100 mL (718 mmol/2.5 eq.) of triethylamine are added all at once. The mixture is brought to 0° C. and a solution of 25.8 mL (315.9 mmol/1.1 eq.) of acryloyl chloride in 270 mL of dichloromethane is poured in dropwise, maintaining the temperature at about 0° C. After 2 hours at 0° C., the mixture is stirred at ambient temperature overnight. Washing with 750 mL of water, 750 mL of 1N hydrochloric acid and 750 mL of water and then drying over magnesium sulphate are then carried out. After filtration and evaporation, the residue is chromatographed over 3.2 kg of silica (eluant: dichloromethane/ethanol: 95/5), followed by recrystallisation from isopropanol. After filtration over a frit and drying in vacuo at 50° C., the desired product is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076325B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-01fa4a3c5f0240519da7d7926605189f
출처 메모uspto-grants-2011_12