Hydrogen Bromide → HCID 18947045, compound
Reaction equation
[Cl:1][C:2]1[S:3][C:4]([Cl:20])=[C:5]2[CH2:9][N:8](S(C3C=CC(C)=CC=3)(=O)=O)[CH2:7][C:6]=12.Br>C(O)(=O)C>[Cl:1][C:2]1[S:3][C:4]([Cl:20])=[C:5]2[CH2:9][NH:8][CH2:7][C:6]=12Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
A mixture of 6.98 g (0.02 mol) of 1,3-dichloro-5-tosyl-5,6-dihydro-4H-thieno[3,4-c]pyrrole and 50 ml of a 33% solution of hydrobromic acid in acetic acid, placed in a sealed tube, is heated at 90° C. in a water bath for 90 min. The reaction mixture is then cooled, and the precipitate formed is filtered off, washed twice with diethyl ether and dried. There are obtained 4.75 g of compound in the hydrobromide form (Melting point >270° C.). Treatment of this salt with sodium carbonate in water produces 3.35 g of base. Melting point: 80.5°-82.5° C.
Workup
- customplaced in a sealed tube
- temperatureThe reaction mixture is then cooled
- customthe precipitate formed
- filtrationis filtered off
- washwashed twice with diethyl ether
- customdried
Sources & evidence
- ORD record
- ord-95d2388e00e14987a1dfb642054ffe0b
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05380742
Reaction notes
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