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Methanol → Methyl 4-phenylpiperidine-4-carboxylate hydrochloride

HRID 1682983
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HRID 1682983 반응식
Cl.[C:2]1([C:8]2([C:14]([OH:16])=[O:15])[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:17]O.O=S(Cl)[Cl:21]>C(OCC)C>[ClH:21].[CH3:17][O:15][C:14]([C:8]1([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH2:9][CH2:10][NH:11][CH2:12][CH2:13]1)=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 426142494-Phenylpiperidine-4-carboxylic acid--hydrogen chloride (1/1)

생성물 1

HCID 3019446Methyl 4-phenylpiperidine-4-carboxylate hydrochloride

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

4-phenyl-piperidine-4-carboxylic acid hydrochloride (from example 20.6) (2.67 g, 11 mmol) and methanol (35 mL) were combined. SOCl2 (0.9 mL, 12.34 mmol, 1.1 eq.) was added dropwise. The reaction was heated at reflux for 18 h. The reaction was concentrated in vacuo to obtain a residue. The residue was slurried in diethyl ether, filtered, and the solids were rinsed with diethyl ether to give the title compound.

후처리

  1. temperatureThe reaction was heated
  2. temperatureat reflux for 18 h
  3. concentrationThe reaction was concentrated in vacuo
  4. customto obtain a residue
  5. filtrationfiltered
  6. washthe solids were rinsed with diethyl ether

출처 및 근거

ORD 기록
ord-5bdd2c66613f4fe880bd72984130e3bc
출처 데이터셋
uspto-grants-1997_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05635510

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