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N,N-Dimethylaniline → 1-Chloro-7-[(4-methoxyphenyl)methoxy]-2,4-dinitro-9(10H)-acridinone

HRID 1584057
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HRID 1584057 반응식
[Cl:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][C:8]([N+:14]([O-:16])=[O:15])=[C:7]([NH:17][C:18]2[CH:23]=[CH:22][C:21]([O:24][CH2:25][C:26]3[CH:31]=[CH:30][C:29]([O:32][CH3:33])=[CH:28][CH:27]=3)=[CH:20][CH:19]=2)[C:3]=1[C:4](O)=[O:5].CN(C)C1C=CC=CC=1.P(Cl)(Cl)(Cl)=O>ClCCCl>[Cl:1][C:2]1[C:3]2[C:4](=[O:5])[C:19]3[C:18](=[CH:23][CH:22]=[C:21]([O:24][CH2:25][C:26]4[CH:31]=[CH:30][C:29]([O:32][CH3:33])=[CH:28][CH:27]=4)[CH:20]=3)[NH:17][C:7]=2[C:8]([N+:14]([O-:16])=[O:15])=[CH:9][C:10]=1[N+:11]([O-:13])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 949N,N-DimethylanilineHCID 24813Phosphorus oxychlorideHCID 13588350HCID 13588350, 화합물

생성물 1

HCID 135883391-Chloro-7-[(4-methoxyphenyl)methoxy]-2,4-dinitro-9(10H)-acridinone

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

To a stirred, ice-cold mixture of 2.67 g of 2-chloro-6-[[4-[(4-methoxyphenyl)methoxy]phenyl]amino]-3,5-dinitrobenzoic acid, 18 ml of 1,2-dichloroethane, and 4.4 ml of N,N-dimethylaniline, was added 0.70 ml of phosphorus oxychloride. After 2.5 hours, the ice bath was removed and the mixture stirred 24 hours at room temperature. The precipitate was collected, washed with water, then with methanol, and dried to provide the title compound, melting above 240° C. with decomposition.

후처리

  1. customthe ice bath was removed
  2. customThe precipitate was collected
  3. washwashed with water
  4. dry with materialwith methanol, and dried

출처 및 근거

ORD 기록
ord-d4115c0ebded45208f7e8f02547d527c
출처 데이터셋
uspto-grants-1985_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04555572

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