Benzyl Bromide → (S)-2-Phthalimido-6-hydroxyhexanoic acid, phenylmethyl ester

HRID 343049

反応式

HRID 343049 の反応式
C(=O)([O-])[O-].[Cs+].[Cs+].[C:7]1(=[O:26])[N:11]([C@@H:12]([CH2:16][CH2:17][CH2:18][CH2:19][OH:20])[C:13]([OH:15])=[O:14])[C:10](=[O:21])[C:9]2=[CH:22][CH:23]=[CH:24][CH:25]=[C:8]12.[CH2:27](Br)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>CN(C)C=O>[C:10]1(=[O:21])[N:11]([C@@H:12]([CH2:16][CH2:17][CH2:18][CH2:19][OH:20])[C:13]([O:15][CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[O:14])[C:7](=[O:26])[C:8]2=[CH:25][CH:24]=[CH:23][CH:22]=[C:9]12

参加物

5

実験手順

A slurry of cesium carbonate (3.819 g, 11.7 mmol.) and (S)-2-phthalimido-6-hydroxyhexanoic acid (6.00 g, 21.6 mmol.) in dimethylformamide (60 ml.) was treated with benzyl bromide (3.30 ml., 4.75 g., 27.7 mmol.). After stirring at room temperature for 2 hours, the mixture was partitioned between ethyl acetate and water. The organic extract was washed with water (twice) and brine, then dried (sodium sulfate), filtered and stripped to give an oil. The oil was flash chromatographed (Merck silica gel, 6/4-ethyl acetate/hexane) to give essentially pure product as a solid. Recrystallization from ethyl acetate/hexane gave 7.173 g. (1st crop) and 394 mg. (2nd crop) for a total of 7.567 g. of pure title product; m.p. 106°-108.5° C.; [α]D =-27.5° (c=1.5, methanol). TLC (75/25 ethyl acetate/hexanes) Rf =0.43.

後処理

  1. customthe mixture was partitioned between ethyl acetate and water
  2. extractionThe organic extract
  3. washwas washed with water (twice) and brine
  4. dry with materialdried (sodium sulfate)
  5. filtrationfiltered
  6. customto give an oil
  7. customchromatographed (Merck silica gel, 6/4-ethyl acetate/hexane)
  8. customto give essentially pure product as a solid
  9. customRecrystallization from ethyl acetate/hexane
  10. customgave 7.173 g

出典と根拠

ORDレコード
ord-51b51440594141e4b127581ce63645c1
出典データセット
uspto-grants-1999_01
特許番号
US05859239

関連ノート

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