Allyl Mercaptan → HCID 21217655, compound
Reaction equation
[Na].[CH2:2]([SH:5])[CH:3]=[CH2:4].[CH2:6]([O:11][C:12]1[N:13]=[N:14][C:15](Cl)=[CH:16][CH:17]=1)[CH2:7][CH2:8][CH2:9][CH3:10]>CO>[CH2:6]([O:11][C:12]1[N:13]=[N:14][C:15]([S:5][CH2:2][CH:3]=[CH2:4])=[CH:16][CH:17]=1)[CH2:7][CH2:8][CH2:9][CH3:10]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1.15 g(0.05 mol) of metallic sodium was dissolved in 75 ml of absolute methanol and then mixed with 4.98 ml(0.05 mol) of allylmercaptan. To this mixture was added 10.03 g(0.05 mol) of 3-(n-pentyloxy)-6-chloropyridazine. The reaction solution was refluxed for 24 hours and then treated according to the same manner as Example 1 to obtain the title compound as a pale yellow needle crystal.
Workup
- temperatureThe reaction solution was refluxed for 24 hours
- additiontreated
Sources & evidence
- ORD record
- ord-74517d8125aa41d19c5f27b7177fe424
- Source dataset
- uspto-grants-1999_08
- Patent number
- US05942511
Reaction notes
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