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(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
ノート
印刷プレビュー

反応式

HRID 970204 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 1068Dimethyl Sulfide溶媒HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-10 °C

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-c0bf7e56bd8245c1a04d08985b2d68bd
出典データセット
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07309714B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート