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Dimethyl Sulfoxide → HCID 178483127, 화합물

HRID 1577566
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HRID 1577566 반응식
[NH2:1]/[C:2](/[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[C:3]1\[C:4](=[O:12])[C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[S:7]\1.[C:19]([O-])(=O)C.C[NH3+].CS(C)=O>CO>[CH3:19][NH:1]/[C:2](/[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[C:3]1\[C:4](=[O:12])[C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[S:7]\1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 679Dimethyl SulfoxideHCID 14420923MethylammoniumacetatHCID 178510717HCID 178510717, 화합물

생성물 1

HCID 178483127HCID 178483127, 화합물수율 58%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 2.53 gm (0.01 mol) of (E)-2-[(amino)phenylmethylene]-benzo[b]thiophen-3(2H)-one, 40.0 gm (0.44 mol) of methylammonium acetate and 10 ml of dimethylsulfoxide was heated for 5 hours to a reaction temperature of 130° to 140° C. Working up was in accordance with Example 65, and the desired compound, m.p. 154°-155° C. (methanol), was obtained with a yield of 58% of theory. The product was identical to that of Example 2 according to elemental analysis and thin-layer chromatogram.

후처리

  1. temperaturewas heated for 5 hours to a reaction temperature of 130° to 140° C

출처 및 근거

ORD 기록
ord-d8cebf0927f74b54ab39a26dc9cb2c24
출처 데이터셋
uspto-grants-1981_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04288437

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