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Ethanol → 4-Ethoxymethyl-2,6-dimethylnitrobenzene

HRID 1577145
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HRID 1577145 반응식
Br[CH2:2][C:3]1[CH:8]=[C:7]([CH3:9])[C:6]([N+:10]([O-:12])=[O:11])=[C:5]([CH3:13])[CH:4]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:20]([OH:22])[CH3:21]>>[CH2:20]([O:22][CH2:2][C:3]1[CH:8]=[C:7]([CH3:9])[C:6]([N+:10]([O-:12])=[O:11])=[C:5]([CH3:13])[CH:4]=1)[CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 11430Potassium CarbonateHCID 205718604-Bromomethyl-2,6-dimethylnitrobenzene

생성물 1

HCID 205718654-Ethoxymethyl-2,6-dimethylnitrobenzene

실험 절차

The product from Step A (19.0 g) is dissolved in ethanol (600 ml) and anhydrous potassium carbonate (32 g) is added. The reaction mixture is stirred at reflux until the reaction is complete by tlc (two hours). The mixture is cooled, and the solids are filtered, washed, and discarded. The filtrate and washings are evaporated to a residue and purified by column chromatography on silica gel, using as eluant cyclohexane/ethyl acetate (97:3 v/v). The desired product, 4-ethoxymethyl-2,6-dimethylnitrobenzene (10.4 g) is isolated as a colorless oil.

후처리

  • temperatureat reflux until the reaction
  • customis complete by tlc (two hours)
  • temperatureThe mixture is cooled
  • filtrationthe solids are filtered
  • washwashed
  • customThe filtrate and washings are evaporated to a residue
  • custompurified by column chromatography on silica gel
  • 출처 및 근거

    ORD 기록
    ord-b7aad892e8e3499c89e4a0223508c013
    출처 데이터셋
    uspto-grants-1981_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04287201

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