Hydrochloric Acid → HCID 18546617, compound
Reaction equation
[OH:1][CH2:2][C:3]([F:28])([F:27])[C:4]([F:26])([F:25])[C:5]([F:24])([F:23])[C:6]([F:22])([F:21])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][C:10]=1[N+:18]([O-:20])=[O:19].[F:29][C:30]1[C:35]([N+:36]([O-:38])=[O:37])=[C:34]([F:39])[C:33]([F:40])=[C:32](F)[C:31]=1[F:42].C(N(CC)CC)C.Cl>CN1C(=O)CCC1.O>[N+:18]([C:10]1[CH:11]=[C:12]([N+:15]([O-:17])=[O:16])[CH:13]=[CH:14][C:9]=1[O:8][CH2:7][C:6]([F:21])([F:22])[C:5]([F:23])([F:24])[C:4]([F:25])([F:26])[C:3]([F:27])([F:28])[CH2:2][O:1][C:32]1[C:31]([F:42])=[C:30]([F:29])[C:35]([N+:36]([O-:38])=[O:37])=[C:34]([F:39])[C:33]=1[F:40])([O-:20])=[O:19]Participants
7
Procedure
1-(6-hydroxy-2,2,3,3,4,4,5,5-octafluorohexyloxy)-2,4-dinitrobenzene (3.7 g) was treated with pentafluoronitrobenzene (2.21 g) and triethylamine (0.96 g) in NMP (5 mL) for 18 hrs at room temperature. The mixture was diluted with water, acidified with hydrochloric acid, and extracted with ethyl ether. The extracts were washed with water, dried (MgS04), concentrated and purified by chromatography to give 4-[6-(2,4-dinitrophenoxy)-2,2,3,3,4,4,5,5-octaflurohexyloxy]-2,3,5,6-tetrafluoronitrobenzene (5.0 g) as an oil.
Workup
- extractionextracted with ethyl ether
- washThe extracts were washed with water
- customdried (MgS04)
- concentrationconcentrated
- custompurified by chromatography
Sources & evidence
- ORD record
- ord-f299c6da0d1e4209b464a4322c2a9494
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06451960B1
Reaction notes
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