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1,2-Bis(4-fluorophenyl)-2-hydroxyethanone → HCID 178456614, 화합물

HRID 2051957
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반응식

HRID 2051957 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH:10]([C:12]2[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=2)O)=O)=[CH:4][CH:3]=1.[CH:19]([NH:22][C:23]([NH2:25])=[S:24])([CH3:21])[CH3:20]>CN(C=O)C>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:25]=[C:23]([SH:24])[N:22]([CH:19]([CH3:21])[CH3:20])[C:10]=2[C:12]2[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1037861,2-Bis(4-fluorophenyl)-2-hydroxyethanoneHCID 1711921Urea, 1-isopropyl-2-thio-

생성물 1

HCID 178456614HCID 178456614, 화합물수율 56.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 30 g (0.121 mole) of 4,4'-difluorobenzoin, 14.3 g (0.121 mole) of N-isopropylthiourea and 100 ml DMF was heated at reflux through molecular sieves for five hours. The mixture was cooled to room temperature and the crystalline product was collected, washed with DMF/water, then water, then dried to give 22.7 g of 4,5-bis(4-fluorophenyl)-1-isopropylimidazole-2-thiol as a pale yellow solid, mp 308°-312°.

후처리

  1. temperaturewas heated
  2. temperatureat reflux through molecular sieves for five hours
  3. customthe crystalline product was collected
  4. washwashed with DMF/water
  5. dry with materialwater, then dried

출처 및 근거

ORD 기록
ord-b125f3dd28b34fc79a6778d4949317ac
출처 데이터셋
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04182769

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