Triethylamine → 1-(Hydroxymethyl)-cyclopentanecarboxylic acid methyl ester

HRID 217242노트

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HRID 217242 반응식
[CH3:1][O:2][C:3]([C:5]1([C:10](O)=[O:11])[CH2:9][CH2:8][CH2:7][CH2:6]1)=[O:4].C(N(CC)CC)C.ClC(OCC(C)C)=O>C1COCC1>[CH3:1][O:2][C:3]([C:5]1([CH2:10][OH:11])[CH2:6][CH2:7][CH2:8][CH2:9]1)=[O:4]

참가 물질

5

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온도
0 °C

실험 절차

To a solution of cyclopentane-1,1-dicarboxylic acid methyl ester (1.00 g, 5.81 mmol) and triethylamine (808 uL, 5.81 mmol) in THF (15 mL) is added isobutyl chloroformate (750 uL, 5.81 mmol) at 0° C. The mixture is stirred at 0° C. for 20 minutes. The mixture is filtrated, and the filtrate is added to a suspension of NaBH4 (242 mg) in THF (15 ml) at 0° C. The mixture is stirred at 0° C. for 3 hours and at room temperature for 12 hours. To the mixture, H2O is added and the mixture is extracted with AcOEt. The organic layer is dried over MgSO4, and concentrated under reduced pressure. The obtained residue is purified by silica gel column chromatography to give 1-hydroxymethyl-cyclopentanecarboxylic acid methyl ester (433 mg, 47%); TLC (hexane/AcOEt, 1:1) Rf 0.43, 1H NMR (400 MHz, chloroform-d) δ ppm 1.61-1.77 (m, 6H), 1.93-2.00 (m, 2H), 2.53 (m, 1H), 3.57 (d, 2H), 3.72 (s, 3H).

후처리

  1. filtrationThe mixture is filtrated
  2. additionthe filtrate is added to a suspension of NaBH4 (242 mg) in THF (15 ml) at 0° C
  3. stirringThe mixture is stirred at 0° C. for 3 hours and at room temperature for 12 hours
  4. additionTo the mixture, H2O is added
  5. extractionthe mixture is extracted with AcOEt
  6. dry with materialThe organic layer is dried over MgSO4
  7. concentrationconcentrated under reduced pressure
  8. customThe obtained residue is purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-1515738fd6d643958dcfa7780a632c16
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08193349B2

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