Dimethylamine → N,N-dimethyl-2-(phenylthio)benzamide

HRID 328878Notes

Reaction equation

HRID 328878 reaction equation
[C:1]1([S:7][C:8]2[CH:16]=[CH:15][CH:14]=[CH:13][C:9]=2[C:10](Cl)=[O:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1(SC2C=CC=CC=2C(O)=O)C=CC=CC=1.S(Cl)(Cl)=O.[CH3:37][NH:38][CH3:39]>C1C=CC=CC=1>[CH3:37][N:38]([CH3:39])[C:10](=[O:11])[C:9]1[CH:13]=[CH:14][CH:15]=[CH:16][C:8]=1[S:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

6

Reactant 4

HCID 674DimethylamineHCID 152102-(Phenylthio)benzoic acidHCID 24386Thionyl ChlorideHCID 2913222-(Phenylsulfanyl)benzoyl chloride

Product 1

HCID 21402688N,N-dimethyl-2-(phenylthio)benzamide

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent2×

Procedure

Following the procedure described in Example 1, 2-(phenylthio)benzoyl chloride is prepared from 0.065 mole of 2-(phenylthio)benzoic acid and excess thionyl chloride. A solution of the oily acid chloride in 50 ml. of benzene is added dropwise with stirring to a solution of 7 g. of dimethylamine in 50 ml. of benzene. The mixture is heated briefly to refluxing. Evaporation of the solvent under reduced pressure leaves N,N-dimethyl-2-(phenylthio)benzamide as the residue.

Workup

  1. temperatureThe mixture is heated briefly
  2. temperatureto refluxing
  3. customEvaporation of the solvent under reduced pressure

Sources & evidence

ORD record
ord-52c36e262bb74d0babc4acd9d434083a
Source dataset
uspto-grants-1977_04
Patent number
US04018830

Reaction notes

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