Benzyl Chloride → (+/-)-6-Benzyloxy-2,5,7,8-tetramethylchroman-2-carboxylic acid

HRID 1415244

反応式

HRID 1415244 の反応式
OC1C(C)=C2C(=C(C)C=1C)OC(C)(C(O)=O)CC2.C(=O)([O-])[O-].[K+].[K+].C(Cl)C1C=CC=CC=1.C([O:40][C:41]([C:43]1([CH3:64])[CH2:52][CH2:51][C:50]2[C:45](=[C:46]([CH3:63])[C:47]([CH3:62])=[C:48]([O:54][CH2:55][C:56]3[CH:61]=[CH:60][CH:59]=[CH:58][CH:57]=3)[C:49]=2[CH3:53])[O:44]1)=[O:42])C1C=CC=CC=1.[OH-].[Na+]>O.CS(C)=O>[CH2:55]([O:54][C:48]1[C:49]([CH3:53])=[C:50]2[C:45](=[C:46]([CH3:63])[C:47]=1[CH3:62])[O:44][C:43]([CH3:64])([C:41]([OH:42])=[O:40])[CH2:52][CH2:51]2)[C:56]1[CH:57]=[CH:58][CH:59]=[CH:60][CH:61]=1

参加物

8

実験手順

To a mixture of 0.5 g. of (±)-6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid and 1.3 g. of anhydrous potassium carbonate in 3 ml. of dimethylsulfoxide was added 1.0 g. of benzyl chloride. This mixture was stirred at 23° overnight to give a solution containing (±)-benzyl-6-benzyloxy-2,5,7,8-tetramethylchroman-2-carboxylate. To this solution was added 3 ml. of 1N sodium hydroxide solution and 2 ml. of dimethylsulfoxide and the resulting 2-phase solution was stirred at 100° for 16 hours. The mixture was cooled, diluted with H2O, washed with ether, acidified with 2N HCl, and extracted with ether. The ether solutions were washed with brine, dried over sodium sulfate and stripped of solvent. The residue was crystallized from ether-30°-60° petroleum ether to give (±)-6-benzyloxy-2,5,7,8-tetramethylchroman-2-carboxylic acid as a white solid, m.p. 154.5°-155°.

後処理

  1. additionTo a mixture of 0.5 g
  2. customto give a solution
  3. additionTo this solution was added 3 ml
  4. temperatureThe mixture was cooled
  5. washwashed with ether
  6. extractionextracted with ether
  7. washThe ether solutions were washed with brine
  8. dry with materialdried over sodium sulfate
  9. customThe residue was crystallized from ether-30°-60° petroleum ether

出典と根拠

ORDレコード
ord-63b72a1d12fa41cb84f4b07b24c2674b
出典データセット
uspto-grants-1977_01
特許番号
US04003919

関連ノート

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