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Methanol → Methyl 1-amino-4-methoxy-4-(methoxymethyl)cyclohexanecarboxylate

HRID 922127
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HRID 922127 반응식
S(Cl)(Cl)=O.Cl.[NH2:6][C:7]1([C:18]([OH:20])=[O:19])[CH2:12][CH2:11][C:10]([O:16][CH3:17])([CH2:13][O:14][CH3:15])[CH2:9][CH2:8]1.[CH3:21]O>>[NH2:6][C:7]1([C:18]([O:20][CH3:21])=[O:19])[CH2:12][CH2:11][C:10]([O:16][CH3:17])([CH2:13][O:14][CH3:15])[CH2:9][CH2:8]1
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참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 904137241-Amino-4-methoxy-4-(methoxymethyl)cyclohexanecarboxylic acid hydrochloride

생성물 1

HCID 71246293Methyl 1-amino-4-methoxy-4-(methoxymethyl)cyclohexanecarboxylate

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온도
40 °C

실험 절차

At 0° C., 4.1 ml (55.60 mmol) of thionyl chloride were added dropwise to 4.70 g of the compound from Example 20A in 50 ml of methanol. The mixture was stirred at 0° C. for 0.5 hours and at 40° C. overnight. After cooling, the mixture was concentrated, the residue was taken up in ethyl acetate and washed with saturated aqueous sodium bicarbonate solution, the aqueous phase was extracted repeatedly with ethyl acetate and the combined organic phases were dried over sodium sulphate, filtered and concentrated. This gave 392 mg (61% of theory from Example 16A) of the title compound as a diastereomer mixture which was reacted without further purification.

후처리

  1. temperatureAfter cooling
  2. concentrationthe mixture was concentrated
  3. washwashed with saturated aqueous sodium bicarbonate solution
  4. extractionthe aqueous phase was extracted repeatedly with ethyl acetate
  5. dry with materialthe combined organic phases were dried over sodium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThis gave 392 mg (61% of theory from Example 16A) of the title compound as a diastereomer mixture which was reacted without further purification

출처 및 근거

ORD 기록
ord-4476164929a843b09942da0cb7dcba47
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09278925B2

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