Benzene → Chloromethyl phenyl sulphide

HRID 2050176Notes

Reaction equation

HRID 2050176 reaction equation
C=O.[ClH:3].[C:4]1([SH:10])C=CC=CC=1.[CH:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[C:11]1([S:10][CH2:4][Cl:3])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Participants

5

Conditions

Temperature
31 °C

Procedure

With stirring, 37.5 grams (1.25 moles) of paraformaldehyde was added to 250 ml of benzene. To the benzene-paraformaldehyde mixture 500 ml of concentrated hydrochloric acid was added slowly at ambient temperature. The mixture was then heated at 31° C. for 30 minutes, and 110 grams of thiophenol was added. Upon complete addition the reaction mixture was heated at 50°-55° C. for 2 hours, then allowed to cool to ambient temperature where it stood for 18 hours. The reaction mixture was separated and the organic layer washed with 250 ml of water. The water wash was extracted with 250 ml of benzene and the two benzene layers were combined. The benzene combination was washed with 300 ml of aqueous saturated sodium chloride, dried with magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to a residue which was further evaporated under high vacuum and distilled to give 115.9 grams (73.2%) of phenylthiomethyl chloride; b.p. 80° C./3 mm. The nmr and the ir spectra were consistent with the assigned structure.

Workup

  1. additionUpon complete addition the reaction mixture
  2. temperaturewas heated at 50°-55° C. for 2 hours
  3. temperatureto cool to ambient temperature where it
  4. customThe reaction mixture was separated
  5. washthe organic layer washed with 250 ml of water
  6. washThe water wash
  7. extractionwas extracted with 250 ml of benzene
  8. washThe benzene combination was washed with 300 ml of aqueous saturated sodium chloride
  9. dry with materialdried with magnesium sulfate
  10. filtrationfiltered
  11. customThe filtrate was evaporated under reduced pressure to a residue which
  12. customwas further evaporated under high vacuum
  13. distillationdistilled

Sources & evidence

ORD record
ord-15347a338e8b4a4e9e1f07ba9d258c47
Source dataset
uspto-grants-1980_04
Patent number
US04200644

Reaction notes

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