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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1246376생성일: 2026년 10월 26일

Triethylamine → (4S)-5,5-Diphenyl-4-(propan-2-yl)-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/1246376

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DiphosgeneHCID 10426—
반응물Sodium HydroxideHCID 14798—
반응물(S)-(-)-2-Amino-3-methyl-1,1-diphenyl-1-butanolHCID 854145—
용매DichloromethaneHCID 6344—
용매Sodium chloride; waterHCID 57417360—
생성물(4S)-5,5-Diphenyl-4-(propan-2-yl)-1,3-oxazolidin-2-oneHCID 983864686.5%

반응 단계

Trichloromethyl chloroformate (2.71 g, 13.7 mmol) was added to a mixture of (S)-2-amino-3-methyl-1,1-diphenyl-1-butanol (2) (3.18 g, 12.45 mmol) and triethylamine (2.68 g, 26.52 mmol) in CH2Cl2 at 0° C. The reaction mixture was stirred for 2 h at the same temperature and then poured into a brine solution (250 ml). The aqueous layer was made basic with NaOH pellets and organic products were extracted into AcOEt (5×200 ml). Combined organic extracts were dried over MgSO4 and concentrated under reduced pressure. The resulting crude product was washed with diethyl ether to obtain the title compound (3) (3.03 g, 86%) as a white solid. m.p. 250–251° C. (liti 250–251° C.). [α]D25=−201.59° (c, 0.0252 in DMSO). δH (DMSO-d6) 0.51 (3H, d, 3J=6.60 Hz, CH3), 0.92 (3H, d, 3J=7.20 Hz, CH3), 1.86 (1H, ds, 3J=2.10 and 6.60 Hz, CH—Me2), 4.46 (1H, d, 3J=6.5 Hz, CH—NH2), 7.24–7.72 (10H, m, Ar—H), 8.14 (1H, s, NH). δC 15.2 and 20.9 (CH3), 29.8 (CH), 64.9 (CH—NHCO), 88.4 (C—O), 125.8, 126.2, 127.9, 128.4, 128.8 and 129.1 (Ar), 140.5 and 146.1 (α-Ar), 158.1 (C═O). Ir 3295 (NH2), 1765 and 1745 (C═O). m/e (CI—NH3) 282 (MH+, 25%), 299 (MNH4+, 8%), 238 (96%), 223 (100%), 72 (100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07126028B1
출처 데이터셋uspto-grants-2006_10
ORD IDord-56149978dbb04527ba3483bc9c2c6d19
출처 메모uspto-grants-2006_10