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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217907생성일: 2026년 10월 23일

tert-Butanol → N-Cbz-4-[(2,3-Dihydroxypropyloxy)phenyl]butylamine

https://huagongshe.com/ko/reaction/217907

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물N-Methylmorpholine N-oxide monohydrateHCID 2724197—
반응물[4-(4-Allyloxyphenyl)butyl]carbamic acid benzyl esterHCID 11551825—
반응물Sodium BisulfiteHCID 23665763—
촉매Osmium TetroxideHCID 30318—
용매Propan-2-one--water (1/1)HCID 18366337—
생성물N-Cbz-4-[(2,3-Dihydroxypropyloxy)phenyl]butylamineHCID 1155979462%

반응 단계

A solution of osmium tetroxide (50 mg, 0.2 mmol) in tert-butanol (8 mL) was added to a solution of 4-methylmorpholine N-oxide monohydrate (1.2 g, 9.1 mmol) in 100 mL (1:1) acetone/water solution and the mixture was stirred for 10 min at room temperature. After this time, 30 (3.1 g, 9.0 mmol) was added in 50 mL (1:1) acetone/water solution. The reaction mixture was stirred at room temperature overnight, then NaHSO3 (0.5 g) was added and the stirring was continued for 15 min. The acetone was evaporated and the pH was adjusted to 5.5 by the addition of 2N HCl then the mixture was extracted with ethyl acetate. The organic fraction was isolated, dried with sodium sulfate, and filtered through silica gel. Compound 31 (2.1 g, 62%) was isolated as a white solid after removing the solvent and drying under vacuum. 1H NMR (300 MHz, DMSO-d6) δ 1.48 (m, 2H), 1.50 (m, 2H), 2.46 (m, 2H), 3.00 (m, 2H), 3.43 (m, 2H), 3.80 (m, 2H), 3.93 (t, 1H), 4.66 (d, 1H), 4.99 (s, 2H), 6.82 (d, 2H), 7.07 (d, 2H), 7.26 (s, 1H), 7.33 (s, 5H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198286B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-a2127e81f42b41ce9e2c3fc910f2cafe
출처 메모uspto-grants-2012_06