Acetonitrile → HCID 53647028, compound
Reaction equation
[F:1][C:2]([F:32])([C:28]([F:31])([F:30])[F:29])[C:3]([F:27])([F:26])[C:4]([F:25])([F:24])[O:5][C:6]([F:23])([F:22])[C:7]([F:21])([F:20])[O:8][C:9]([F:19])([F:18])[CH2:10][O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16]Br.[CH2:33]([C:43]1[CH:44]=[N:45][C:46]([C:49]2[CH:54]=[CH:53][C:52]([OH:55])=[CH:51][CH:50]=2)=[N:47][CH:48]=1)[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH3:42].C(=O)([O-])[O-].[K+].[K+].C(#N)C>CN(C)C=O>[CH2:33]([C:43]1[CH:44]=[N:45][C:46]([C:49]2[CH:50]=[CH:51][C:52]([O:55][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][O:11][CH2:10][C:9]([O:8][C:7]([F:21])([F:20])[C:6]([F:23])([F:22])[O:5][C:4]([F:25])([F:24])[C:3]([F:27])([F:26])[C:2]([F:32])([F:1])[C:28]([F:31])([F:30])[F:29])([F:19])[F:18])=[CH:53][CH:54]=2)=[N:47][CH:48]=1)[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH3:42]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Using essentially the procedure of Comparative Example A, the title compound was prepared by combining 5-(2-(2 -(nonafluorobutoxy)tetrafluoroethoxy)-2,2 -difluoroethoxy)-l-bromopentane (4.4 g, 7.6 mmol), 5 -decyl-2-(4-hydroxyphenyl)pyrimidine (2.0 g, 6.4 mmol), potassium carbonate (0.5 g, 10 mmol), acetonitrile (20 mL), and dimethyl formamide (20 mL). The resulting crude product was isolated and purified essentially as in Comparative Example A to yield 4.98 g.
Sources & evidence
- ORD record
- ord-95b000fda0b4468783226de71552a97b
- Source dataset
- uspto-grants-1999_01
- Patent number
- US05855812
Reaction notes
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