Pyridinium chloride → HCID 13290184, compound
Reaction equation
[Cl:1][C:2]1[C:3]([O:16]C)=[CH:4][C:5]2[C:9]3[CH2:10][CH2:11][CH2:12][CH2:13][C:8]=3[S:7][C:6]=2[C:14]=1[Cl:15].Cl.N1C=CC=CC=1>>[Cl:1][C:2]1[C:3]([OH:16])=[CH:4][C:5]2[C:9]3[CH2:10][CH2:11][CH2:12][CH2:13][C:8]=3[S:7][C:6]=2[C:14]=1[Cl:15]Participants
3
Procedure
A mixture of 4.2 g of 3,4-dichloro-6,7,8,9-tetrahydro-2-methoxydibenzothiophene and 40 g of pyridine hydrochloride is stirred at 190°-195° under nitrogen for 2 hours. The cooled mixture is triturated with water and the solid product is collected. Recrystallization from ether-pentane after decolorization with charcoal gave 3.6 g of 3,4-dichloro-6,7,8,9-tetrahydro-2-hydroxydibenzothiophene as off-white crystals, mp 103°-105°.
Workup
- customThe cooled mixture is triturated with water
- customthe solid product is collected
- customRecrystallization from ether-pentane after decolorization with charcoal
Sources & evidence
- ORD record
- ord-c182918ceb6245038bd528b8c6f5f32a
- Source dataset
- uspto-grants-1987_06
- Patent number
- US04672138
Reaction notes
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