Thiophenol → 4-Tert-Butylbenzenethiol

HRID 1659505Notes

Reaction equation

HRID 1659505 reaction equation
[C:1]1([SH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:8][C:9](=[CH2:11])[CH3:10]>>[C:9]([C:4]1[CH:5]=[CH:6][C:1]([SH:7])=[CH:2][CH:3]=1)([CH3:11])([CH3:10])[CH3:8]

Participants

3

Conditions

Temperature
70 °C

Procedure

To a mixture of 1100 grams (10.0 moles) of thiophenol, and 300 grams of boron trifluoride-phosphoric acid complex was slowly added, with stirring, 620 grams (10.9 moles) of isobutylene at 0° C. After addition was complete the mixture was stirred at 0°-10° C. for two hours. The mixture was then heated to 70° C. and stirred at 70°-75° C. for two hours. The reaction mixture was cooled to 25° C. and the organic layer was separated from the lower catalyst layer and added to 500 ml of toluene. The toluene layer was washed four times with 1000-ml portions of water and then dried with magnesium sulfate. The toluene was evaporated from the mixture in vacuo and the residue was distilled in a 10-tray column to give 1120 grams of 4-(tert-butyl)thiophenol, b.p. 58°-60°/1.00 mm (yield 68%). The nmr spectrum agreed with the structure. The residue from the above distillation was 470 grams of tert-butyl 4-(tert-butyl)phenyl sulfide. Neuworth et al (1963) report b.p. 120°/20 mm for 4-(tert-butyl)thiophenol.

Workup

  1. additionwas slowly added
  2. customat 0° C
  3. additionAfter addition
  4. stirringwas stirred at 0°-10° C. for two hours
  5. stirringstirred at 70°-75° C. for two hours
  6. temperatureThe reaction mixture was cooled to 25° C.
  7. customthe organic layer was separated from the lower catalyst layer
  8. additionadded to 500 ml of toluene
  9. washThe toluene layer was washed four times with 1000-ml portions of water
  10. dry with materialdried with magnesium sulfate
  11. customThe toluene was evaporated from the mixture in vacuo
  12. distillationthe residue was distilled in a 10-tray column

Sources & evidence

ORD record
ord-fc09c60990cf4f2bad57404ccf6b1192
Source dataset
uspto-grants-1981_12
Patent number
US04304735

Reaction notes

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