반응식
[F:1][C:2]([F:10])([F:9])[C:3]#[C:4][C:5]([F:8])([F:7])[F:6].[CH3:11][NH:12][N:13]=[C:14](Br)[C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][CH:16]=1.C(N(CC)CC)C>C1(C)C=CC=CC=1>[Cl:21][C:18]1[CH:17]=[CH:16][C:15]([C:14]2[C:3]([C:2]([F:10])([F:9])[F:1])=[C:4]([C:5]([F:8])([F:7])[F:6])[N:12]([CH3:11])[N:13]=2)=[CH:20][CH:19]=1참가 물질
5
반응 조건
- 온도
- 20 °C
실험 절차
5.7 g (41 nmol) of gaseous hexafluoro-2-butyne were passed at below (-50)° C. into a suspension, cooled to (-70)° C., of 9 g (36 mmol) of α-bromo-4-chlorobenzaldehyde methylhydrazone in 100 ml of toluene. The mixture was subsequently heated to (-25)° C., and 8.4 g (83 mmol) of triethylamine were added dropwise at this temperature. After the mixture had been stirred for 2 hours at this temperature and for a further 16 hours at approx. 20° C., it as washed with water, dried over magnesium sulfate and finally concentrated.
후처리
- temperatureinto a suspension, cooled to (-70)° C
- temperatureThe mixture was subsequently heated to (-25)° C
- washit as washed with water
- dry with materialdried over magnesium sulfate
- concentrationfinally concentrated
출처 및 근거
- ORD 기록
- ord-336f424022a04588bed5af5300766373
- 출처 데이터셋
- uspto-grants-2000_04
- 특허 번호
- US06054412
연결된 노트
불러오는 중…