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Diethyl (ethoxymethylene)malonate → HCID 20207465, 화합물

HRID 542896
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HRID 542896 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:6]=[C:7]([OH:9])[CH:8]=1)[NH2:5].C(O[CH:13]=[C:14]([C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:15]([O:17][CH2:18][CH3:19])=[O:16])C>C(O)C>[CH2:23]([O:22][C:20]([C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:13][NH:5][C:4]1[CH:3]=[C:2]([OH:1])[CH:8]=[C:7]([OH:9])[CH:6]=1)=[O:21])[CH3:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6871Diethyl (ethoxymethylene)malonateHCID 4107515-Aminobenzene-1,3-diol

생성물 1

HCID 20207465HCID 20207465, 화합물수율 78.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 3,5-dihydroxyaniline (2.0 g), 2-ethoxy-1,1-bis(ethoxycarbonyl)ethene (3.0 g) and ethanol (10 ml) was left to stand at room temperature for 2 days. The resulting solid was filtered off, dissolved in dimethylsulphoxide (20 ml) and then treated with water (100 ml). The resulting solid was washed with water, to give 1,1-bis(ethoxycarbonyl)-2-(3,5-dihydroxyphenylamino)ethene (3.2 g), m.p. 190°-192° C.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. waitwas left
  2. filtrationThe resulting solid was filtered off
  3. dissolutiondissolved in dimethylsulphoxide (20 ml)
  4. additiontreated with water (100 ml)
  5. washThe resulting solid was washed with water

출처 및 근거

ORD 기록
ord-f87a7a8ee59749e1b4a6fac1317f8799
출처 데이터셋
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04659727

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