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4-Toluenesulfonyl chloride → 2-Nitro-4-piperidin-1-ylmethyl-benzoic acid methyl ester

HRID 1640969
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반응식

HRID 1640969 반응식
[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10]O)=[CH:6][C:5]=1[N+:12]([O-:14])=[O:13].C(N(CC)CC)C.C1(C)C=CC(S(Cl)(=O)=O)=CC=1.[NH:34]1[CH2:39][CH2:38][CH2:37][CH2:36][CH2:35]1>ClCCl>[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][N:34]2[CH2:39][CH2:38][CH2:37][CH2:36][CH2:35]2)=[CH:6][C:5]=1[N+:12]([O-:14])=[O:13]
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참가 물질

6

반응물 4

HCID 73974-Toluenesulfonyl chlorideHCID 8082PiperidineHCID 8471TriethylamineHCID 22672700Methyl 4-(hydroxymethyl)-2-nitrobenzoate

생성물 1

HCID 667368402-Nitro-4-piperidin-1-ylmethyl-benzoic acid methyl ester수율 45.5%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

To a solution of 4-hydroxymethyl-2-nitro-benzoic acid methyl ester (2.0 g, 9.47 mmol) in dry dichloromethane (80 mL) under argon, at room temperature, triethylamine (1.6 mL, 10.9 mmol, 1.15 eq.) and then p-toluenesulfonyl chloride (2.08 g, 10.9 mmol, 1.15 eq.) were added. The reaction mixture was stirred at room temperature for 1 h, then piperidine (1.6 mL, 18.94 mmol, 2 eq.) was added and the mixture stirred for additional 24 hours. The solvent was evaporated and the residue purified by flash chromatography on silica gel, using dichloromethane/ethanol 95:5 as eluant, affording 1.2 g of the title compound.

후처리

  1. stirringthe mixture stirred for additional 24 hours
  2. customThe solvent was evaporated
  3. customthe residue purified by flash chromatography on silica gel

출처 및 근거

ORD 기록
ord-41dbc85d833e4ccf908f958ecae04f6b
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08114865B2

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