홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

(4S)-3-[(2E)-But-2-enoyl]-4-phenyl-1,3-oxazolidin-2-one → (4S)-3-[(3R)-3-(4-Fluorophenyl)butanoyl]-4-phenyl-1,3-oxazolidin-2-one

HRID 970204
노트
인쇄 미리보기

반응식

HRID 970204 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([Mg]Br)=[CH:4][CH:3]=1.[C:10]([N:15]1[C@@H:19]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH2:18][O:17][C:16]1=[O:26])(=[O:14])/[CH:11]=[CH:12]/[CH3:13]>C1COCC1.CSC>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:12]([CH3:13])[CH2:11][C:10]([N:15]2[C@@H:19]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:18][O:17][C:16]2=[O:26])=[O:14])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 5469245(4S)-3-[(2E)-But-2-enoyl]-4-phenyl-1,3-oxazolidin-2-oneHCID 178418676HCID 178418676, 화합물

생성물 1

HCID 69364772(4S)-3-[(3R)-3-(4-Fluorophenyl)butanoyl]-4-phenyl-1,3-oxazolidin-2-one

시약·촉매·용매 2

HCID 1068Dimethyl Sulfide용매HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
-10 °C

실험 절차

To a stirred solution of copper(II)bromide dimethylsulfide complex (6.85 g, 33.3 mmol) in anhydrous THF (60 mL) and dimethylsulfide (30 mL) was added 4-fluorophenylmagnesium bromide (30.0 mL, 1.0 M in THF, 30.0 mmol) at −40° C. The resultant mixture was stirred at −40° C. for 30 min, then warmed to −10° C. The product from Step A (1.18 g, 5.10 mmol) in THF (30 mL) was added to the above reaction mixture over 1 h at −10° C. The resultant mixture was stirred at −10° C. for 2 h, then slowly warmed to room temperature and stirred at room temperature for 12 h. The reaction was quenched by slow addition of saturated aqueous ammonium chloride solution. The organic phase was separated and the aqueous phase was extracted with two portions of ethyl acetate. The combined organic layers were washed with brine and concentrated in vacuo. Purification by flash chromatography (silica gel, 80:20 hexanes/ethyl acetate) afforded the desired product.

후처리

  1. temperatureslowly warmed to room temperature
  2. customThe reaction was quenched by slow addition of saturated aqueous ammonium chloride solution
  3. customThe organic phase was separated
  4. extractionthe aqueous phase was extracted with two portions of ethyl acetate
  5. washThe combined organic layers were washed with brine
  6. concentrationconcentrated in vacuo
  7. customPurification by flash chromatography (silica gel, 80:20 hexanes/ethyl acetate)

출처 및 근거

ORD 기록
ord-c0bf7e56bd8245c1a04d08985b2d68bd
출처 데이터셋
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07309714B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트