돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1036521생성일: 2026년 10월 24일

Toluene → (R)-4-methyl-4-(6-(4-pentylcyclohexyloxy)naphthalen-2-yl)oxazolidin-2-one

https://huagongshe.com/ko/reaction/1036521

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물TetrahydrofuranHCID 8028—
반응물TriphenylphosphineHCID 11776—
반응물4-PentylcyclohexanolHCID 41076—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물(R)-4-(6-hydroxynaphthalen-2-yl)-4-methyloxazolidin-2-oneHCID 51066623—
생성물(R)-4-methyl-4-(6-(4-pentylcyclohexyloxy)naphthalen-2-yl)oxazolidin-2-oneHCID 67413569—

반응 단계

In a 40 mL vial, 4-Pentyl-cyclohexanol (1144.4 mg, 0.0067202 mol) was diluted with tetrahydrofuran (30.0 mL, 0.370 mol, Acros) and subsequently (R)-4-(6-hydroxynaphthalen-2-yl)-4-methyloxazolidin-2-one (1.4924 g, 0.0061350 mol) and triphenylphosphine (2105.5 mg, 0.0080275 mol) were added and the mixture was stirred. Diethyl Azodicarboxylate in toluene (2.6 mL, 0.0086326 mol, Aldrich) was added, and the mixture was then stirred at room temperature for 38 h. The reaction mixture was evaporated to dryness and chromatographed 0-100% EtOAc/Hexanes (adsorbed onto silica gel). Isolated was 0.6142 g (18%) in approx 70% purity, the remainder being reduced DEAD reagent.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08546359B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-50a3bf3819c54405854819d6f6526ab2
출처 메모uspto-grants-2013_10