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Sodium methanethiolate → 5-Chloro-2-methylthio-3-pyridinecarbonitrile

HRID 368282
Notes
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Reaction equation

HRID 368282 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]#[N:10])[CH:5]=[N:6][C:7]=1Cl.[CH3:11][S-:12].[Na+]>CS(C)=O>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]#[N:10])[C:5]([S:12][CH3:11])=[N:6][CH:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 4378561Sodium methanethiolateHCID 128784645,6-Dichloropyridine-3-carbonitrile

Product 1

HCID 232882615-Chloro-2-methylthio-3-pyridinecarbonitrileYield 71%

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Procedure

5,6-Dichloro-3-pyridinecarbonitrile (1.73 g, 0.01 mol) was dissolved with stirring in dimethyl sulphoxide (25 mL) and sodium methanethiolate (0.77 g, 0.011 mol) added. The reaction mixture was stirred at room temperature for two hours and poured onto ice (100 g). The mixture was extracted with dichloromethane (50 mL), and the organic extract washed with water (100 mL), and brine, and dried over anhydrous sodium sulphate. Evaporation of the solvent under reduced pressure and recrystallisation of the residue from ethyl acetate:hexane gave the desired product (1.3 g, 71%) as a cream solid, MP 147-9° C.

Workup

  1. additionpoured onto ice (100 g)
  2. extractionThe mixture was extracted with dichloromethane (50 mL)
  3. extractionthe organic extract
  4. washwashed with water (100 mL), and brine
  5. dry with materialdried over anhydrous sodium sulphate
  6. customEvaporation of the solvent
  7. customunder reduced pressure and recrystallisation of the residue from ethyl acetate

Sources & evidence

ORD record
ord-726385f03c9446b5ae77352515a07821
Source dataset
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06133294

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes