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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 547882생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/547882

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07939658B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-060a98dad3504ba0ab5ede5dc0e8435b
출처 메모uspto-grants-2011_05