Water → HCID 10633484, compound
Reaction equation
[CH2:1]([C:7]1[CH:13]=[CH:12][C:10]([NH2:11])=[CH:9][CH:8]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[S-:14][C:15]#[N:16].[K+].BrBr.O>C(O)(=O)C>[NH2:16][C:15]1[S:14][C:12]2[CH:13]=[C:7]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])[CH:8]=[CH:9][C:10]=2[N:11]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
In a 2 liter-reaction vessel, 50.0 g (0.28 M) of p-hexylaniline, 54.8 g (0.56 M) of potassium thiocyanate and 400 ml of acetic acid were placed and cooled below 10° C. To the mixture, a solution of 45.0 g of bromine in 135 ml of acetic acid was added dropwise in 40 minutes below 10° C. under strong stirring, followed by reaction for 1.5 hours below 10° C. After the reaction, 500 ml of water was poured into the reaction mixture, followed by heating to dissolve the resultant precipitate. The resultant solution was filtered under heating. Ammonia water was added to the filtrate until the resultant solution became basic, followed by cooling with ice to precipitate a crystal. The crystal was recovered by filtration, followed by washing and drying to obtain a crude product. The crude product was recrystallized from a mixture solvent of n-hexane/benzene (1/1) to obtain 33.0 g of 2-amino-6-hexylbenzothiazole (Yield: 49.9%).
Workup
- temperaturecooled below 10° C
- customfollowed by reaction for 1.5 hours below 10° C
- additionwas poured into the reaction mixture
- temperatureby heating
- filtrationThe resultant solution was filtered
- temperatureunder heating
- additionAmmonia water was added to the filtrate until the resultant solution
- temperatureby cooling with ice
- customto precipitate a crystal
- filtrationThe crystal was recovered by filtration
- washby washing
- customdrying
- customto obtain a crude product
- customThe crude product was recrystallized from a mixture solvent of n-hexane/benzene (1/1)
Sources & evidence
- ORD record
- ord-29209cefe7c3408dbf54b100600db0b3
- Source dataset
- uspto-grants-1993_12
- Patent number
- US05268123
Reaction notes
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