Benzyl mercaptan → Methyl 4-(benzylthio)-2-chlorobenzoate

HRID 1808201Notes

Reaction equation

HRID 1808201 reaction equation
[Cl:1][C:2]1[CH:11]=[C:10](F)[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].C(=O)([O-])[O-].[Cs+].[Cs+].[CH2:19]([SH:26])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.C(OCC)(=O)C>CS(C)=O>[CH2:19]([S:26][C:10]1[CH:9]=[CH:8][C:3]([C:4]([O:6][CH3:7])=[O:5])=[C:2]([Cl:1])[CH:11]=1)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

Participants

6

Reactant 4

HCID 7509Benzyl mercaptanHCID 8857Ethyl AcetateHCID 10796Cesium carbonateHCID 2763551Methyl 2-Chloro-4-fluorobenzoate

Product 1

HCID 22387852Methyl 4-(benzylthio)-2-chlorobenzoateYield 95%

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Conditions

Temperature
50 °C

Procedure

Methyl 2-chloro-4-fluorobenzoate (1.92 g, 10.2 mmol, 1 eq), cesium carbonate (3.74 g, 11.5 mmol, 0.13 eq) and benzyl mercaptan (1.3 g, 10.5 mmol, 1.03 eq) were combined in dimethyl sulphoxide (20 ml) and the reaction mixture heated at 50° C. for 4 hours. The reaction mixture was poured into ethyl acetate (10 ml) then washed with water (10 ml). The organic phase was dried over sodium sulphate, evaporated to yield the title compound as pink oil (2.82 g, 9.63 mmol, 95%).

Workup

  1. washthen washed with water (10 ml)
  2. dry with materialThe organic phase was dried over sodium sulphate
  3. customevaporated

Sources & evidence

ORD record
ord-929df6f4113a4aeaa3a7fbf682102a1f
Source dataset
uspto-grants-2013_01
Patent number
US08357711B2

Reaction notes

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