Ethyl Acetate → 5-(2-Benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl ester

HRID 9295노트

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HRID 9295 반응식
[CH3:1][O:2][C:3]([CH:5]1[CH2:10][CH:9]([CH2:11][CH2:12][O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:8][CH2:7][CH:6]1O)=[O:4].O=S(Cl)Cl.C1CCN2C(=NCCC2)CC1.CCOC(C)=O>N1C=CC=CC=1>[CH3:1][O:2][C:3]([C:5]1[CH2:10][CH:9]([CH2:11][CH2:12][O:13][CH2:14][C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH2:8][CH2:7][CH:6]=1)=[O:4]

참가 물질

6

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온도
55 °C

실험 절차

A solution of 5-(2-benzyloxy-ethyl)-2-hydroxy-cyclohexanecarboxylic acid methyl ester (Intermediate R2, 0.72 g, 2.48 mmol) in pyridine (10 mL) was treated with SOCl2 (0.73 mL, 12.4 mmol) at −20° C. The mixture was allowed to react for 15 m and was then warmed to 55° C. for 16 h. The solvents were removed under vacuum and the residue was diluted in ether at 0° C. The solution was quenched with water, washed with 1M HCl, 5% NaOH and brine. The organic material was dried over MgSO4 filtered and freed of solvent. The mixture was diluted with benzene and water was removed by azeotropic distillation under vacuum. The residue was dissolved in benzene (15 mL) and DBU (0.76 mL, 5 mmol) was added. The mixture was reacted for 30 m at rt. After work-up and chromatography on SiO2 with 20% EtOAc:Hx 5-(2-benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl ester (Intermediate R3) was isolated 0.56 g (82%).

후처리

  1. customto react for 15 m
  2. customThe solvents were removed under vacuum
  3. additionthe residue was diluted in ether at 0° C
  4. customThe solution was quenched with water
  5. washwashed with 1M HCl, 5% NaOH and brine
  6. dry with materialThe organic material was dried over MgSO4
  7. filtrationfiltered
  8. additionThe mixture was diluted with benzene and water
  9. customwas removed by azeotropic distillation under vacuum
  10. dissolutionThe residue was dissolved in benzene (15 mL)
  11. customThe mixture was reacted for 30 m at rt

출처 및 근거

ORD 기록
ord-a212ef8076d6461486f10c4b5443e7f8
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07091232B2

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