Dimethylformamide → HCID 86644385, compound
Reaction equation
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[S:3][CH:2]1[CH2:10][C:11]([OH:13])=O.S(Cl)(Cl)=O.C[N:19]([CH:21]=O)C>C1(C)C=CC=CC=1>[S:3]1[C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=2[S:1][CH:2]1[CH2:10][C:11]([NH:19][C:21]1[CH:8]=[CH:9][CH:4]=[CH:5][CH:6]=1)=[O:13]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
To a solution of 2-(benzo[1,3]dithiol-2-yl)acetic acid (1.35 g) in toluene (30 mL) were added thionyl chloride (0.600 mL) and DMF (catalytic amount) at room temperature, and the mixture was stirred at 80° C. for 2 hours. The reaction mixture was concentrated under reduced pressure. To the residue was added acetonitrile (30 mL), and then was added dropwise a solution of aniline (1.54 g) in acetonitrile (10 mL) under ice-cooling. The mixture was stirred at the same temperature for 1 hour and then at room temperature for 3 hours, and then concentrated under reduced pressure. To the residue was added 1N hydrochloric acid (50 mL), and the mixture was stirred at room temperature for 0.5 hour. The formed crystals were collected by filtration, washed with water, filtered, and then dried to obtain 2-(benzo[1,3]dithiol-2-yl)-N-(phenyl)acetamide (1.83 g) as a white crystal.
Workup
- concentrationThe reaction mixture was concentrated under reduced pressure
- additionTo the residue was added acetonitrile (30 mL)
- additionwas added dropwise a solution of aniline (1.54 g) in acetonitrile (10 mL) under ice-
- temperaturecooling
- stirringThe mixture was stirred at the same temperature for 1 hour
- waitat room temperature for 3 hours
- concentrationconcentrated under reduced pressure
- additionTo the residue was added 1N hydrochloric acid (50 mL)
- stirringthe mixture was stirred at room temperature for 0.5 hour
- filtrationThe formed crystals were collected by filtration
- washwashed with water
- filtrationfiltered
- customdried
Sources & evidence
- ORD record
- ord-373ea586fe6a432ab5b905823db03092
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318981B2
Reaction notes
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