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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 429725생성일: 2026년 10월 26일

Water → 1-(2,3,4,5-Tetrahydro-1,4-benzoxazepin-4-yl)ethan-1-one

https://huagongshe.com/reaction/429725

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TetrahydrofuranHCID 8028—
반응물Sodium HydroxideHCID 14798—
반응물2,3,4,5-Tetrahydro-1,4-benzoxazepin-5-oneHCID 340629—
반응물Aluminium lithium hydrideHCID 21226445—
생성물1-(2,3,4,5-Tetrahydro-1,4-benzoxazepin-4-yl)ethan-1-oneHCID 18352685—

반응 단계

To a solution of 1.5 g of 2,3,4,5-tetrahydro-1,4-benzoxazepin-5-one in 20 ml of tetrahydrofuran, was added 0.5 g of lithium aluminium hydride by portion, and the mixture was heated and refluxed for 2 hours. The reaction mixture was cooled to the room temperature. To the reaction mixture were added dropwise 1 ml of water and 0.8 ml of 10% aqueous solution of sodium hydroxide, and the mixture was stirred for 6 hours at room temperature. After the resultant solid mater was removed by filtration, the filtrate was concentrated under reduced pressure, and 20 ml of dichloromethane was added to the residue. The solution was dried over anhydrous sodium sulfate, then to the solution was added 0.94 ml of acetic anhydride, the mixture was stirred for 15 minutes at room temperature. The solvent was distilled off under reduced pressure, and the resulting oily residue was purified by means of column chromatography (developing solvent: dichloromethane-ethyl acetate=5:1 (V/V)) to give 1.8 g of 4-acetyl-2,3,4,5-tetrahydro-1,4-benzoxazepine as a colorless oily substance. The compound was used in the following steps without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06319916B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-06aa02204c14478e86751a6121926c1f
출처 메모uspto-grants-2001_11