m,alpha-Dichlorotoluene → 4-{[(3-Chlorophenyl)methyl]sulfanyl}pyridine
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5]Cl.[SH:10][C:11]1[CH:16]=[CH:15][N:14]=[CH:13][CH:12]=1>C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][S:10][C:11]1[CH:16]=[CH:15][N:14]=[CH:13][CH:12]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-Chlorobenzyl chloride (1.61 g) and 4-mercaptopyridine (1.11 g) in ethanol (10 ml) were heated at reflux for 4 hours and cooled. Crystals which precipitated were removed by filtration and dried to give the title compound as the hydrochloride (1.3 g) mp 222°-224° C. (Found: C, 52.6; H, 4.3; N, 5.1. C12H10ClNS requires C, 52.95; H, 4.1; N, 5.1%).
Workup
- temperatureat reflux for 4 hours
- temperaturecooled
- customCrystals which precipitated
- customwere removed by filtration
- customdried
Sources & evidence
- ORD record
- ord-764cf685f22145018645c892bd187c1d
- Source dataset
- uspto-grants-1981_12
- Patent number
- US04304781
Reaction notes
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