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Formaldehyde → 5-IMIDIZOLIDINONE, 1-(o-CHLORO-p-SULFAMOYLPHENYL)-3-PHENYL-

HRID 1658202
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인쇄 미리보기

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HRID 1658202 반응식
[C:1]1([NH:7][CH2:8][C:9]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([S:18](=[O:21])(=[O:20])[NH2:19])=[CH:14][C:13]=2[Cl:22])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:23]=O>C(O)C.O>[C:1]1([N:7]2[CH2:8][C:9](=[O:10])[N:11]([C:12]3[CH:17]=[CH:16][C:15]([S:18](=[O:21])(=[O:20])[NH2:19])=[CH:14][C:13]=3[Cl:22])[CH2:23]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 712FormaldehydeHCID 21528839HCID 21528839, 화합물

생성물 1

HCID 407115-IMIDIZOLIDINONE, 1-(o-CHLORO-p-SULFAMOYLPHENYL)-3-PHENYL-

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

2-Phenylamino-N-(2-chloro-4-sulphamoylphenyl)-acetamide (34.0g) was dissolved in ethanol (300 ml) and paraformaldehyde (6.0g) in water (600 ml) added. The mixture was refluxed 4 hours, cooled and worked up as in Example 2(c) to yield 20 g m.p. 206°

후처리

  1. temperatureThe mixture was refluxed 4 hours
  2. temperaturecooled
  3. customto yield 20 g m.p. 206°

출처 및 근거

ORD 기록
ord-c4004da1393c4548bcfe63241977d6ec
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03963706

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