CAUTION: This preparation should be conducted in an
efficient fume cupboard.
- Place 50g (0.33 mol) of anhydrous aluminium chloride (1) Into a 1-litre three-necked flask and 200 ml (2.25 mol) of dry benzene (CAUTION); cool in a bath of crushed ice.
- Stir the mixture and add 50g (59 ml, 0.54 mol) of t-butyl chloride from the dropping funnel during 4-5 hours; the first addition should be 3-4 ml in order to prevent the benzene from freezing.
- Maintain the mixture at a temperature of 0-5 °C by the addition of salt to the ice, if necessary.
- When all the t-butyl chloride has been run in, continue the stirring for 1 hour longer.
- Remove the separatory funnel and add 200g of finely crushed ice in small portions with stirring; finally add 100 ml of cold water to complete the decomposition of the intermediate addition compound.
- Arrange the flask for steam distillation and steam distil the resulting reaction mixture.
- Transfer the steam distillate to a separatory funnel, remove the upper hydrocarbon layer, extract the water layer with two 50 ml portions of ether and combine the extracts with the upper layer.
- Dry with magnesium sulphate, distil off the ether on a water bath and fractionally distil the residue twice, using a well-lagged column.
- Collect the t-butylbenzene at 165-170 °C. The yield is 45g (62%). Pure t-butylbenzene boils at 168.5 °C.
- Note the characteristic absorptions for the aromatic system at c. 3050 cm⁻¹ , at 1600, 1590 and 1500 cm⁻¹ and at c. 700 and 765 cm⁻¹ for a monosubstituted nucleus. The t-butyl group shows characteristic carbon-hydrogen stretching absorptions at c. 2950 cm⁻¹.
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