Water → 4-methylbenzoic acid [(R)-2-methylheptyl]ester

HRID 483902

반응식

HRID 483902 반응식
C[C@@H:2](O)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH3:10][C:11]1[CH:19]=[CH:18][C:14]([C:15](Cl)=[O:16])=[CH:13][CH:12]=1.[OH2:20].[C:21]1(C)C=CC=CC=1>N1C=CC=CC=1>[CH3:21][C@H:7]([CH2:6][CH2:5][CH2:4][CH2:3][CH3:2])[CH2:8][O:20][C:15](=[O:16])[C:14]1[CH:18]=[CH:19][C:11]([CH3:10])=[CH:12][CH:13]=1

참가 물질

6

실험 절차

40 g (0.31 moles) of a commercially available (R)-2-octanol was dissolved in 100 ml of pyridine. The mixture was cooled and 47.93 g (0.31 moles) of a commercially available 4-methylbenzoic chloride was added thereto while cooling. The mixture was then allowed to react with stirring at 50° to 60° C. for 2 hours. On completion of the reaction, 300 ml of water and 300 ml of toluene were added, and after vigorous stirring, the toluene layer was separated out and washed with 6N HCl. Washing was continued until this layer was neutral. This toluene layer was dried with anhydrous magnesium sulfate, after which the toluene was distilled away. The residue was further subjected to evaporation under reduced pressure at 144° to 146° C. (2 mm Hg) and the distillate recovered, whereby 70.37 g of the objective 4-methylbenzoic acid [(R)-2-methylheptyl]ester was obtained.

후처리

  1. temperatureThe mixture was cooled
  2. temperaturewhile cooling
  3. customto react
  4. additionwere added
  5. customafter vigorous stirring, the toluene layer was separated out and
  6. washwashed with 6N HCl
  7. washWashing
  8. dry with materialThis toluene layer was dried with anhydrous magnesium sulfate
  9. distillationafter which the toluene was distilled away
  10. customThe residue was further subjected to evaporation under reduced pressure at 144° to 146° C. (2 mm Hg)
  11. distillationthe distillate recovered

출처 및 근거

ORD 기록
ord-9e291465847147e39d44b0f7d0979f3e
출처 데이터셋
uspto-grants-1993_07
특허 번호
US05227512

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