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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39367생성일: 2026년 10월 25일

Dimethyl Sulfoxide → tert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamate

https://huagongshe.com/reaction/39367

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물tert-butyl N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]carbamateHCID 2733675—
용매DichloromethaneHCID 6344—
생성물tert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamateHCID 6998013100.3%

반응 조건

온도-78 °C

반응 단계

Oxalyl chloride in anhydrous CH2Cl2 (2.0M, 6.0 mL, 12.0 mmol) was treated with dimethylsulfoxide (1.0 mL, 14.1 mmol) in anhydrous CH2Cl2 (3 mL) dropwise over 5 minutes at −78° C. under a dry N2 atmosphere. The mixture was stirred at −78° C. for 15 minutes and then treated with (2S)-2-(tert-butoxycarbonylamino)-3-phenyl-1-propanol (2.0 g, 8.0 mmol) in anhydrous CH2Cl2 (6 mL) dropwise over 10 minutes. The mixture was stirred at −78° C. for 30 minutes and then treated with triethylamine (4.4 mL, 31.7 mmol) in anhydrous CH2Cl2 (6 mL) dropwise over 10 minutes. The mixture was allowed to slowly warm to ambient temperature, stirred for 1 hour, diluted with CH2Cl2 (100 mL), washed with 10% aqueous citric acid (50 mL), water (50 mL), saturated NaHCO3 (50 mL), dried over Na2SO4, filtered, and the solvent removed under reduced pressure to provide the title compound as an off-white crystalline solid (2.0 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524753B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-2670f69763064b539b76dacfdfbfdf25
출처 메모uspto-grants-2013_09