1,3-Cyclohexanedicarboxylic acid → 3-Oxabicyclo[3.3.1]nonane-2,4-dione

HRID 352256

반응식

HRID 352256 반응식
[CH:1]1([C:10]([OH:12])=[O:11])[CH2:6][CH2:5][CH2:4][CH:3]([C:7]([OH:9])=O)[CH2:2]1>C(OC(=O)C)(=O)C>[CH:1]12[CH2:2][CH:3]([CH2:4][CH2:5][CH2:6]1)[C:7](=[O:9])[O:12][C:10]2=[O:11]

참가 물질

3

반응 조건

온도
140 °C

실험 절차

A suspension of 1,3-cyclohexanedicarboxylic acid (490 g, 2.88 mol) in acetic anhydride (1500 ml) was heated to 140° C., refluxing for 2 hours. Acetic anhydride was then removed with distillation (oil bath 180° C). To the residue was added acetic anhydride (1000 ml) and refluxed at 140° C. for 1 hour. The acetic anhydride was removed again with distillation (under house vacuum, about 50° C.). After crystals appeared, the mixture was cooled to room temperature and MTBE (400 ml) was added. The mixture was then cooled to 0-5° C. The crystals were filtered, washed with MTBE (250 ml), and dried under house vacuum to give the title compound (382 g). The filtrate was concentrated to a residue and suspended in MTBE (100 ml) to give the second crop of the title compound (14.0 g). The total yield was 396 g (90.5%). Mp 138-140° C.

후처리

  1. temperaturerefluxing for 2 hours
  2. customAcetic anhydride was then removed with distillation (oil bath 180° C)
  3. additionTo the residue was added acetic anhydride (1000 ml)
  4. temperaturerefluxed at 140° C. for 1 hour
  5. customThe acetic anhydride was removed again with distillation (under house vacuum, about 50° C.)
  6. temperaturethe mixture was cooled to room temperature
  7. additionMTBE (400 ml) was added
  8. temperatureThe mixture was then cooled to 0-5° C
  9. filtrationThe crystals were filtered
  10. washwashed with MTBE (250 ml)
  11. customdried under house vacuum

출처 및 근거

ORD 기록
ord-1a22a9b284944989b8ea87f7105a94c8
출처 데이터셋
uspto-grants-2004_06
특허 번호
US06743794B2

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