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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1450183생성일: 2026년 10월 25일

Ammonium Hydroxide → 8-Chloro-11-(4-benzyl-1-piperazinyl)-dibenz[b,f][1,4]oxazepine

https://huagongshe.com/reaction/1450183

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium HydroxideHCID 14923—
반응물1-BenzylpiperazineHCID 75994—
반응물2-Chlorodibenz(b,f)-1,4-oxazepin-11(10H)-oneHCID 76619—
촉매Titanium TetrachlorideHCID 24193—
용매TolueneHCID 1140—
생성물8-Chloro-11-(4-benzyl-1-piperazinyl)-dibenz[b,f][1,4]oxazepineHCID 988745195.6%

반응 단계

To a stirred solution of 8-chloro-10,11-dihydro-dibenz[b,f][1,4]oxazepin-11-one (0.3 g; 1.22 mmol) in dry toluene (10 mL) at room temperature was added 1-benzyl piperazine (1.0 mL; 5.61 mmol; Aldrich) followed by the dropwise addition of TiCl4 (1M in toluene, 1.47 mL; 1.47 mmol). The reaction mixture was refluxed for 2 hours, cooled to room temperature and then poured into an ammonium hydroxide solution (30%, 50 mL). The resulting mixture was extracted with dichloromethane (4×50 mL), and the combined organic phases were then dried (K2CO3) and concentrated. Purification of the product was conducted on silica gel using ethyl acetate:hexane (5:1→4:1) as the eluant to give 0.471 g (95%) of the title compound as a yellow solid; m.p. 50°-52° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05602120
출처 데이터셋uspto-grants-1997_02
ORD IDord-5670831b8985425885dfe469db6ea6a7
출처 메모uspto-grants-1997_02