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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 473849생성일: 2026년 10월 24일

Pyridine → 7-bromo-2,3-dihydro-1,4-benzoxazepine-4(5H)-carbonyl chloride

https://huagongshe.com/ko/reaction/473849

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물PhosgeneHCID 6371—
반응물DiisopropylethylamineHCID 81531—
반응물7-Bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochlorideHCID 66820137—
용매DichloromethaneHCID 6344—
생성물7-bromo-2,3-dihydro-1,4-benzoxazepine-4(5H)-carbonyl chlorideHCID 86672020101.7%

반응 단계

7-bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride (3.0 g, 11.34 mmol) was suspended in dichloromethane (30 mL) followed by addition of DIPEA (3 mL, 34 mmol) and pyridine (4 mL, 49 mmol) and the resulting partially heterogeneous mixture was added portionwise over 5 minutes to a 0° C. cooled solution of phosgene (20 W % in toluene, 15 mL, 28 mmol) in dichloromethane (15 mL). The resulting mixture was then allowed to slowly warm to room temperature over 30 minutes then concentrated. The residue was partitioned with ethyl acetate and water and the organic phase washed twice with 1M aqueous hydrochloric acid then brine, dried over anhydrous magnesium sulfate, filtered and concentrated to give 7-bromo-2,3-dihydro-1,4-benzoxazepine-4(5H)-carbonyl chloride (3.35 g) as a pale yellow oil. MS (EI) for C10H9BrClNO2: 292 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637499B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-28ce653894fe44dab97a9617993ac516
출처 메모uspto-grants-2014_01