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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 363309생성일: 2026년 10월 24일

Acetic Acid → 5-(3-Chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepine

https://huagongshe.com/ko/reaction/363309

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물WaterHCID 962—
반응물5-(3-Chloropropanoyl)-10,11-dihydro-5H-dibenzo[b,f]azepineHCID 606961—
반응물Sodium borohydrideHCID 4311764—
용매TetrahydrofuranHCID 8028—
생성물5-(3-Chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepineHCID 28677938.3%

반응 단계

To a solution of 3-chloro-1-(10,11-dihydro-5H-dibenz[b,f]azepin-5-yl)-1-propanone (14.0 g, 0.044 mol) in tetrahydrofuran (150 ml) at 0° C., sodium borohydride (6.66 g, 0.176 mol) was added, followed by dropwise addition of glacial acetic acid (10.0 ml). The resulting mixture was stirred at room temperature overnight and then heated at reflux temperature for 2 h. More sodium borohydride (6.50 g, 172 mmol) and then borontrifluoride diethyl etherate (20.0 ml, 0.163 mol) were added and heating at reflux temperature was continued for 20 h. Water (350 ml) was cautiously added and the phases were separated. The aqueous phase was extracted with toluene (3×100 ml). The combined organic phases were washed with brine (3×100 ml), dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (100 g) using a gradient of heptane and ethyl acetate (10:0→10:2), to give 4.58 g (38%) of 5-(3-chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepine as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05874428
출처 데이터셋uspto-grants-1999_02
ORD IDord-943a4bf634e54b0b94c84c125de361c2
출처 메모uspto-grants-1999_02