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

HRID 264980

반응식

HRID 264980 반응식
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

참가 물질

5

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-826b6d2780a949cbba296ed865bdfdc3
출처 데이터셋
uspto-grants-1997_07
특허 번호
US05646276

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