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Tetraglyme → 2-(4-Methoxy-3-nitrophenylamino)ethanol

HRID 1721164
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HRID 1721164 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[C:4]([N+:10]([O-:12])=[O:11])[CH:3]=1.[OH-].[Ca+2].[OH-].C[O:17][CH2:18][CH2:19]OCCOCCOCCOC.ClC(OCCCl)=O>COCCOC>[OH:17][CH2:18][CH2:19][NH:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[C:4]([N+:10]([O-:12])=[O:11])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8925TetraglymeHCID 123052-Chloroethyl chloroformateHCID 123071Benzenamine, 4-methoxy-3-nitro-HCID 6093208Calcium Hydroxide

생성물 1

HCID 144537412-(4-Methoxy-3-nitrophenylamino)ethanol

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

A mixture of 168.2 g of 4-amino-2-nitroanisole, 42.8 g of calcium hydroxide and 5 g of tetraethylene glycol dimethylether in 1500 g of aqueous monoethylene glycol dimethylether is reacted in accordance with the instructions of Example 1 with 150 g of 2-chloroethyl chloroformate and, after separation of the phases, with 370.6 g of 50% strength potassium hydroxide. After working up analogously to Example 1, yellow-red crystals are obtained.

후처리

  1. customafter separation of the phases
  2. customare obtained

출처 및 근거

ORD 기록
ord-20b4fec4bd15430c94461196959bfef9
출처 데이터셋
uspto-grants-1996_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05508467

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