2-Fluoroethanol → HCID 178523748, 화합물
반응식
[F:1][CH2:2][CH2:3][OH:4].CC(C)([O-])C.[K+].Cl[C:12]1[N:30]=[C:29]([Cl:31])[CH:28]=[CH:27][C:13]=1[C:14]([NH:16][CH:17]1[CH2:22][CH2:21][CH:20]([C:23]([F:26])([F:25])[F:24])[CH2:19][CH2:18]1)=[O:15]>C1COCC1.O>[Cl:31][C:29]1[CH:28]=[CH:27][C:13]([C:14]([NH:16][C@H:17]2[CH2:18][CH2:19][C@H:20]([C:23]([F:24])([F:25])[F:26])[CH2:21][CH2:22]2)=[O:15])=[C:12]([O:4][CH2:3][CH2:2][F:1])[N:30]=1참가 물질
6
실험 절차
2-Fluoroethanol (380 μL, 6.45 mmol) is added to potassium tert-butoxide (730 mg, 6.16 mmol) in THF (60 mL) and stirred for 5 min at rt. After the addition of 2,6-dichloro-N-(4-trifluoromethyl-cyclohexyl)-nicotinamide (2.00 g, 5.86 mmol) the reaction mixture is stirred for 1 h hour at rt, then diluted with water and concentrated. The residue is stirred in ice water, the precipitate is filtered off and dried.
후처리
- stirringis stirred for 1 h hour at rt
- concentrationconcentrated
- stirringThe residue is stirred in ice water
- filtrationthe precipitate is filtered off
- customdried
출처 및 근거
- ORD 기록
- ord-dc7ec1cc6de448e2b416d666e5bd0b3e
- 출처 데이터셋
- uspto-grants-2013_11
- 특허 번호
- US08586604B2
반응 노트
불러오는 중…