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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493081생성일: 2026년 10월 27일

2(3H)-Benzoxazolone → 3-(3-amino-3-methyl-butyl)-3H-benzoxazol-2-one

https://huagongshe.com/reaction/493081

반응식

참여 물질

역할이름HCID투입량
반응물2(3H)-BenzoxazoloneHCID 6043—
반응물Sodium hydrideHCID 24758—
반응물Sodium BicarbonateHCID 516892—
반응물tert-butyl N-(4-amino-2-methylbutan-2-yl)carbamateHCID 45072487—
반응물Tert-butyl [1,1-dimethyl-3-(2-oxobenzooxazol-3-yl)propyl]carbamateHCID 57435843—
촉매Tetrabutylammonium IodideHCID 67553—
용매Ethyl AcetateHCID 8857—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
생성물3-(3-amino-3-methyl-butyl)-3H-benzoxazol-2-oneHCID 57435838—

반응 단계

tert-butyl[1,1-dimethyl-3-(2-oxo-benzoxazol-3-yl)-propyl]-carbamate: 4.0 g (29.6 mmol) benzoxazol-2-one are dissolved in 40 mL DMPU and cooled with an ice bath. Under protective gas 897 mg (95%; 35.5 mmol) sodium hydride is added batchwise to this solution. The reaction mixture is heated to ambient temperature and then stirred for another hour. 9.85 g (44.4 mmol) tert-butyl (3-amino-1,1-dimethyl-propyl)-carbamate and 1.97 g (5.3 mmol) tetrabutylammonium iodide are added and the mixture is stirred overnight. The reaction is stopped by the careful addition of sodium hydrogen carbonate solution. Ethyl acetate is added, the aqueous phase is separated off and extracted repeatedly with ethyl acetate. The combined organic phases are washed with sodium chloride solution, dried with sodium sulphate and evaporated down. Purification of the residue by column chromatography (silica gel; petroleum ether/ethyl acetate=7:3) yields the desired product. Yield 4.1 g (43%); mass spectroscopy: [M+H]+=321.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534789B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-829931ec9cb540ec95496c98b668fbba
출처 메모uspto-grants-2009_05