4'-Hydroxyacetophenone → 4-acetylphenyl 3-tert-butoxycarbonyl-2,2-dimethyloxazolidine-4-(R)-carboxylate

HRID 1724721ノート

反応式

HRID 1724721 の反応式
[C:1]([O:5][C:6]([N:8]1[C@@H:12]([C:13]([OH:15])=[O:14])[CH2:11][O:10][C:9]1([CH3:17])[CH3:16])=[O:7])([CH3:4])([CH3:3])[CH3:2].C1(N=C=NC2CCCCC2)CCCCC1.CN(C1C=CC=CN=1)C.O[C:43]1[CH:48]=[CH:47][C:46]([C:49](=[O:51])[CH3:50])=[CH:45][CH:44]=1>C(OCC)(=O)C>[C:1]([O:5][C:6]([N:8]1[C@@H:12]([C:13]([O:15][C:43]2[CH:48]=[CH:47][C:46]([C:49](=[O:51])[CH3:50])=[CH:45][CH:44]=2)=[O:14])[CH2:11][O:10][C:9]1([CH3:17])[CH3:16])=[O:7])([CH3:4])([CH3:2])[CH3:3]

参加物

6

実験手順

At 0° C., 3-tert-butoxycarbonyl-2,2-dimethyloxazolidine-4-(R)-carboxylic acid (1.0 g) is dissolved in ethyl acetate (25 ml), dicyclohexylcarbodiimide (DCC; 1.26 g) is then added and the reaction mixture is subjected to agitation for 45 minutes at 0° C. Dimethylaminopyridine (DMAP; 100 mg) and 4′-hydroxyacetophenone (565 mg) are successively added, the reaction mixture is then left to return to room temperature. After 5 hours of agitation, the mixture is filtered and the filtrate is washed with a sodium hydrogen carbonate saturated solution, then with a sodium chloride saturated solution. The organic phase is dried on MgSO4, filtered and concentrated. The obtained orange oil is purified by chromatography on silica to obtain the desired product as a transparent oil (940 mg).

後処理

  1. waitthe reaction mixture is then left
  2. customto return to room temperature
  3. waitAfter 5 hours of agitation
  4. filtrationthe mixture is filtered
  5. washthe filtrate is washed with a sodium hydrogen carbonate saturated solution
  6. customThe organic phase is dried on MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe obtained orange oil is purified by chromatography on silica

出典と根拠

ORDレコード
ord-f7a900afe54647e698a35ba0b75d4dfd
出典データセット
uspto-grants-2009_02
特許番号
US07488755B2

反応ノート

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