Trifluoromethanesulfonic acid → 1-Methyladamantane

HRID 1283906Notes

Reaction equation

HRID 1283906 reaction equation
[CH:1]12[CH2:11][CH:7]3[CH:8](C[CH2:10]1)[CH:3]([CH2:4][CH2:5][CH2:6]3)[CH2:2]2.F[C:13](F)(F)S(O)(=O)=O>>[CH3:13][C:5]12[CH2:4][CH:3]3[CH2:2][CH:1]([CH2:11][CH:7]([CH2:8]3)[CH2:6]1)[CH2:10]2

Participants

3

Conditions

Temperature
80 °C

Procedure

A mixture of 7.5 g (0.05 mole) of tricyclo[5.3.1.03,8 ]-undecane (II) and 76 g (0.5 mole) of trifluoromethanesulfonic acid was heated at 80°C. for 30 hours under agitation. The reaction mixture was allowed to cool and then poured over 200 ml of ice water. The organic layer was separated and the water layer was extracted with methylene chloride. The methylene chloride extract was combined with the organic layer, and the mixture was washed with a saturated aqueous solution of sodium hydrogencarbonate and then with water, and dried over anhydrous sodium sulfate. Methylene chloride was distilled off and the residue was sublimed to obtain 6.8 g (yield: 90 wt.%) of 1-methyladamantane (II). All of the IR, NMR and MS spectra of the product were in agreement with those of the authentic sample.

Workup

  1. temperatureto cool
  2. customThe organic layer was separated
  3. extractionthe water layer was extracted with methylene chloride
  4. extractionThe methylene chloride extract
  5. washthe mixture was washed with a saturated aqueous solution of sodium hydrogencarbonate
  6. dry with materialwith water, and dried over anhydrous sodium sulfate
  7. distillationMethylene chloride was distilled off

Sources & evidence

ORD record
ord-cf60af9886924e808a18935731c4f44f
Source dataset
uspto-grants-1976_08
Patent number
US03976706

Reaction notes

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