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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 254088생성일: 2026년 10월 26일

Dicyclohexylcarbodiimide → (4S)-3-[({[2-(4-Methoxyphenyl)-5,5-dimethyl-1,3-dioxan-2-yl]methyl}thio)acetyl]-4-phenyl-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/254088

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2-Oxazolidinone, 4-phenyl-, (4S)-HCID 730424—
반응물({[2-(4-Methoxyphenyl)-5,5-dimethyl-1,3-dioxan-2-yl]methyl}thio)acetic acidHCID 66842966—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물(4S)-3-[({[2-(4-Methoxyphenyl)-5,5-dimethyl-1,3-dioxan-2-yl]methyl}thio)acetyl]-4-phenyl-1,3-oxazolidin-2-oneHCID 66843104—

반응 조건

온도0 °C

반응 단계

({[2-(4-Methoxyphenyl)-5,5-dimethyl-1,3-dioxan-2-yl]methyl}thio)acetic acid (5.4 g, 16.5 mmol) was dissolved in dry CH2Cl2 (80 ml) and cooled to 0° C. N,N′-dicyclohexylcarbodiimide (DCC, 3.76 g; 18.2 mmol) in 20 ml of CH2Cl2 and 4-(dimethylamino)pyridine (DMAP, 4.04 g, 33.1 mmol) were added and the mixture was stirred at 0° C. for 30 minutes. (S)-(+)-4-Phenyl-2-oxazolidinone (2.69 g, 16.5 mmol) was added and the mixture was stirred at room temperature for 17 h. The mixture was filtered, concentrated under reduced pressure and purified by flash-chromatography (hexane:EtOAc 4:1 then 2:1). This afforded 5.69 g (73%) of the title compound as a white solid. 1H-NMR (CDCl3, 200 MHz): δ 0.6 (s, 3H), 1.3 (s, 3H), 2.8 (s, 2H), 3.4 (s, 4H), 3.8 (s, 2H), 3.8 (s, 3H), 4.3 (dd, 1H), 4.7 (t, 1H), 5.4 (dd, 1H), 6.9 (d, 2H), 7.3 (m, 7H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07871998B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-abcfa00923de4b1cb8e133ee79f1aa82
출처 메모uspto-grants-2011_01