Dimethyl Sulfoxide → HCID 13067089, compound
Reaction equation
[F:1][C:2]1[CH:20]=[CH:19][CH:18]=[CH:17][C:3]=1[C:4]([C:6]1[CH:11]=[C:10]([Cl:12])[CH:9]=[CH:8][C:7]=1[CH:13]=[CH:14][C:15]#[N:16])=[O:5].S([CH:31]([N+:33]#[C-])C)(C1C=CC(C)=CC=1)(=O)=O.CS(C)=O.[H-].[Na+].[CH3:41][CH2:42]OCC>O>[F:1][C:2]1[CH:20]=[CH:19][CH:18]=[CH:17][C:3]=1[C:4]([C:6]1[CH:11]=[C:10]([Cl:12])[CH:9]=[CH:8][C:7]=1[C:13]1[C:14]([C:31]#[N:33])=[CH:15][NH:16][C:41]=1[CH3:42])=[O:5]Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 34.5 g (121 mmole) of 3-[2-(2-fluorobenzoyl)-4-chlorophenyl]-2-propenenitrile, 25.3 g (121 mole) of 1-tosylethyl isocyanide, 200 ml of dimethyl sulfoxide and 400 ml of ether was added dropwise to a suspension of 8.9 g (184 mmole) of 50% sodium hydride in mineral oil and 450 ml of ether. When the addition was complete stirring was continued for 2 hr. The mixture was diluted with water and the ether layer was separated. The aqueous solution was extracted with ether. The combined ether extracts were washed with water, dried over anhydrous sodium sulfate, and concentrated at reduced pressure to give a dark oil. Crystallization from ether gave off-white crystals. A small portion was recrystallized from a mixture of methylene chloride and ether to give colorless prisms, mp 201°-202°.
Workup
- additionWhen the addition
- customthe ether layer was separated
- extractionThe aqueous solution was extracted with ether
- washThe combined ether extracts were washed with water
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated at reduced pressure
- customto give a dark oil
- customCrystallization from ether
- customgave off-white crystals
- customA small portion was recrystallized from a mixture of methylene chloride and ether
- customto give colorless prisms, mp 201°-202°
Sources & evidence
- ORD record
- ord-e9355da7639244919f6fac574736abd3
- Source dataset
- uspto-grants-1982_10
- Patent number
- US04354973
Reaction notes
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