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Diisobutylaluminum hydride → Ethyl 4-(hydroxymethyl)piperidine-1-carboxylate

HRID 586137
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HRID 586137 반응식
C[O:2][C:3]([CH:5]1[CH2:10][CH2:9][N:8]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:7][CH2:6]1)=O.CC(C[AlH]CC(C)C)C>C(Cl)Cl>[CH2:14]([O:13][C:11]([N:8]1[CH2:9][CH2:10][CH:5]([CH2:3][OH:2])[CH2:6][CH2:7]1)=[O:12])[CH3:15]
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참가 물질

4

반응물 2

HCID 14487Diisobutylaluminum hydrideHCID 434038731-Ethyl 4-methyl piperidine-1,4-dicarboxylate

생성물 1

HCID 19773576Ethyl 4-(hydroxymethyl)piperidine-1-carboxylate

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
-78 °C

실험 절차

The above ester (12.8 g, 59.5 mmol, 1.0 equiv) was dissolved in 50 mL of dry CH2Cl2 under Ar and cooled to −78° C. A 1 Molar solution of DIBAL-H in CH2Cl2 (149 mL, 149 mmol, 2.5 equiv) was added dropwise over a 30 min period. The cold bath was removed and the reaction solution allowed to warm to ambient temperature. At this time EtOAc (10 mL) was added dropwise to quench the excess DIBAL-H. 100 mL of 1H HCl (aq) was added dropwise over a 30 min period with rapid stirring. The resulting mixture was filtered on a pad of diatomaceous earth and the filtrate was dried over Na2SO4, decanted and concentrated to yield 4-hydroxymethyl-piperidine-1-carboxylic acid ethyl ester as a nearly colorless oil that was used without further purification.

후처리

  1. customThe cold bath was removed
  2. temperatureto warm to ambient temperature
  3. additionAt this time EtOAc (10 mL) was added dropwise
  4. customto quench the excess DIBAL-H
  5. addition100 mL of 1H HCl (aq) was added dropwise over a 30 min period with rapid stirring
  6. filtrationThe resulting mixture was filtered on a pad of diatomaceous earth
  7. dry with materialthe filtrate was dried over Na2SO4
  8. customdecanted
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e35f36f07016443db1cd096e6f5f1fcd
출처 데이터셋
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06936606B2

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