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Ammonium Chloride → Ethyl 4-hydroxy-4-methylcyclohexane-1-carboxylate

HRID 58891
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HRID 58891 반응식
[O:1]=[C:2]1[CH2:7][CH2:6][CH:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:4][CH2:3]1.[Li][CH3:14].[NH4+].[Cl-]>C(OCC)C>[OH:1][C:2]1([CH3:14])[CH2:7][CH2:6][CH:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:4][CH2:3]1
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참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 317638Ethyl 4-oxocyclohexanecarboxylateHCID 178418348HCID 178418348, 화합물

생성물 1

HCID 21911966Ethyl 4-hydroxy-4-methylcyclohexane-1-carboxylate수율 41%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
-60 °C

실험 절차

To a solution of ethyl 4-oxocyclohexanecarboxylate (4.00 g, 23.5 mmol) in diethyl ether (80 mL) was added MeLi (37.6 mL, 1M in diethyl ether) at −60° C. under nitrogen atmosphere. The reaction mixture was stirred at −60° C. for 30 min. Saturated aqueous NH4Cl (50 mL) was added and the resulting mixture was extracted with EtOAc (100 mL×2). The combined organic layers were washed with brine (150 mL) and water (150 mL), dried over anhydrous sodium sulfate, and concentrated. The residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=10:1) to afford ethyl 4-hydroxy-4-methylcyclohexanecarboxylate (1.8 g, 41% yield) as an oil.

후처리

  1. extractionthe resulting mixture was extracted with EtOAc (100 mL×2)
  2. washThe combined organic layers were washed with brine (150 mL) and water (150 mL)
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationconcentrated
  5. customThe residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=10:1)

출처 및 근거

ORD 기록
ord-5683a11f2fe443e6839b40159d080476
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434761B2

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