P-Toluenesulfonylhydrazide → 1,2-Di-(methoxycarbonyl)-4-ethylidene-cyclohexane

HRID 2248079노트

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HRID 2248079 반응식
[C:1]([C:4]1[CH2:5][CH:6]([C:14]([O:16][CH3:17])=[O:15])[CH:7]([CH2:12][CH:13]=1)[C:8]([O:10][CH3:11])=[O:9])(=O)[CH3:2].S(NN)(C1C=CC(C)=CC=1)(=O)=O>C(O)C>[CH3:11][O:10][C:8]([CH:7]1[CH2:12][CH2:13][C:4](=[CH:1][CH3:2])[CH2:5][CH:6]1[C:14]([O:16][CH3:17])=[O:15])=[O:9]

참가 물질

4

반응물 2

HCID 15303P-ToluenesulfonylhydrazideHCID 13453483Dimethyl 1,2,3,6-tetrahydro-4-acetyl-phthalate

생성물 1

HCID 540253811,2-Di-(methoxycarbonyl)-4-ethylidene-cyclohexane수율 80%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

17 g of dimethyl 1,2,3,6-tetrahydro-4-acetyl-phthalate, prepared as described in Example 1, was refluxed in anhydrous ethanol with 14.6 g of tosylhydrazine. After removal of the solvent, 24 g of dimethyl 1,2,3,6-tetrahydro-4-(1-tosylhydraaono-ethyl)-phthalate (IV) crystallized from water m.p. 162°-163° C. m/z 408 (M+.). This compound was dissolved in chloroform, and treated at 0° C. with 14 ml of catechol borane. Sodium acetate was added to the reaction mixture, which was then refluxed. After washing with water, the solvent was evaporated off and the residue was purified by chromatography on a column of silica gel giving 10 g of the title compound (yield 80%): m/z 226 (M+.); PMR (CDCl3): inter alia δ 1.6 (d, J=8 Hz, CH3 --CH=), 5.3 (q, J=8 Hz, CH3 --CH=).

후처리

  1. customAfter removal of the solvent, 24 g of dimethyl 1,2,3,6-tetrahydro-4-(1-tosylhydraaono-ethyl)-phthalate (IV)
  2. customcrystallized from water m.p. 162°-163° C. m/z 408 (M+.)
  3. dissolutionThis compound was dissolved in chloroform
  4. additiontreated at 0° C. with 14 ml of catechol borane
  5. additionSodium acetate was added to the reaction mixture, which
  6. temperaturewas then refluxed
  7. washAfter washing with water
  8. customthe solvent was evaporated off

출처 및 근거

ORD 기록
ord-31af6b2d06d348d7a1b39ac57828ef6e
출처 데이터셋
uspto-grants-1991_08
특허 번호
US05037970

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