Acetic Acid → 8-Chlorodibenzo[b,f]thiepin-3-carboxylic acid
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[S:11][C:10]3[CH:12]=C(C#N)[CH:14]=[CH:15][C:9]=3[CH:8]=[CH:7][C:6]=2[CH:18]=1.S(=O)(=O)(O)O.[C:24]([OH:27])(=[O:26])[CH3:25]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[S:11][C:10]3[CH:12]=[C:25]([C:24]([OH:27])=[O:26])[CH:14]=[CH:15][C:9]=3[CH:8]=[CH:7][C:6]=2[CH:18]=1Participants
4
Procedure
550 Mg. 8-chloro-3-cyanodibenzo[b,f]-thiepin is refluxed for 16 hours in a mixture of 15 cc. acetic acid and 15 cc. 50% aqueous sulfuric acid. The reaction mixture is cooled down and the product filtered, washed with water and dried to yield 485 mg. (82% of the pure acid, m.p. 302°-304° C.
Workup
- temperatureThe reaction mixture is cooled down
- filtrationthe product filtered
- washwashed with water
- customdried
- customto yield 485 mg
Sources & evidence
- ORD record
- ord-e0bf797692724134a55ac243abb7ba2d
- Source dataset
- uspto-grants-1985_08
- Patent number
- US04536507
Reaction notes
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