Hydrogen Bromide → HCID 18947065, compound
Reaction equation
[C:1]([C:4]1[S:5][CH:6]=[C:7]2[CH2:11][N:10](S(C3C=CC(C)=CC=3)(=O)=O)[CH2:9][C:8]=12)([OH:3])=[O:2].[BrH:22]>C(O)(=O)C>[BrH:22].[C:1]([C:4]1[S:5][CH:6]=[C:7]2[CH2:11][NH:10][CH2:9][C:8]=12)([OH:3])=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
A mixture of 0.5 g (1.54 mmol) of 1-carboxy-5-tosyl-5,6-dihydro-4H-thieno[3,4-c]pyrrole and 5 ml of a 33% solution of hydrobromic acid in acetic acid, placed in a sealed tube, is heated at 60° C. in a water bath for 15 min. The reaction mixture is then cooled, the precipitate formed is filtered, washed twice with diethyl ether and dried. 0.32 g of product is obtained in the hydrobromide form. Yield 83%. Melting point: 281.3°-281.7° C.
Workup
- customplaced in a sealed tube
- temperatureThe reaction mixture is then cooled
- customthe precipitate formed
- filtrationis filtered
- washwashed twice with diethyl ether
- customdried
Sources & evidence
- ORD record
- ord-2287cbf3cb854a82a8e957af7c0084b0
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05380742
Reaction notes
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