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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2179951생성일: 2026년 10월 26일

Methanol → [(3R)-3-Hydroxy-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl ester

https://huagongshe.com/reaction/2179951

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Ethyl AcetateHCID 8857—
반응물Borane;tetrahydrofuranHCID 2723981—
반응물Tert-butyl N-[3-oxo-3-(1,3-thiazol-2-YL)propyl]carbamateHCID 69802122—
용매2-MethylpentaneHCID 7892—
용매TetrahydrofuranHCID 8028—
생성물[(3R)-3-Hydroxy-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl esterHCID 6980379667.5%

반응 조건

온도-10 °C

반응 단계

To a solution of (S)-3-methyl-CBS-oxazaborolidine (1M solution in toluene, 0.43 ml) in dry tetrahydrofuran (30 ml) at −10° C. under nitrogen, was added borane-tetrahydrofuran complex (1M in tetrahydrofuran, 2.58 ml) and stirred at −10° C. for 15 minutes. A solution of [3-oxo-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl ester (1.1 g, 4.3 mmol) in dry tetrahydrofuran (20 ml) was added dropwise over 45 minutes and the resulting mixture was allowed to warm up to room temperature over 16 h. Methanol (10 ml) was added and the mixture was stirred at room temperature for 15 minutes before the solvent was removed at reduced pressure. Methanol (10 ml) was again added and removed at reduced pressure to leave a crude yellow oil. Flash chromatography (silica, 25 to 100% ethyl acetate in isohexane) gave 0.75 g of a clear gum (67%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06887871B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-6abf6e0174e14b47a6980028814fe921
출처 메모uspto-grants-2005_05