Acetic Acid → Hydrochloric Acid
Reaction equation
[Cl:1][C:2]1[C:3]([Cl:19])=[CH:4][C:5]2[S:10][CH2:9][CH2:8]C(C#N)(O[Si](C)(C)C)[C:6]=2[CH:18]=1.[C:20]([OH:23])(=[O:22])[CH3:21]>>[ClH:1].[Cl:1][C:2]1[C:3]([Cl:19])=[CH:4][C:5]2[S:10][CH2:9][CH2:8][CH:21]([C:20]([OH:23])=[O:22])[C:6]=2[CH:18]=1Participants
4
Procedure
Following the procedure of Example 2, 6,7-dichloro-4-cyano-4-trimethylsilyloxy-3,4-dihydro-2H-1-benzothiopyran (7.5 g.) and stannous chloride dihydride (30 g.) were reacted in glacial acetic acid (30 ml.) and concentrated hydrochloric acid (30 ml.) to form 6,7-dichloro-3,4-dihydro-2H-1-benzothiopyran-4-carboxylic acid.
Sources & evidence
- ORD record
- ord-024ebf539e3f4d2dad176d817518278c
- Source dataset
- uspto-grants-1980_07
- Patent number
- US04210663
Reaction notes
Loading…