HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066039Generated: October 29, 2026
Diphenylmethane → 4,4'-Di-tert-butyldiphenylmethane
https://huagongshe.com/reaction/2066039
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenylmethane | HCID 7580 | — |
| Reactant | tert-BUTYL CHLORIDE | HCID 10486 | — |
| Catalyst | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 4,4'-Di-tert-butyldiphenylmethane | HCID 1652739 | 139.8% |
Reaction Steps
In a 500-ml flask, to a mixture of 16.8 g (100 mmol) of diphenylmethane and 21.3 g (230 mmol) of tert-butyl chloride, 67 mg (0.5 mmol) of anhydrous AlCl3 were added, at room temperature, under vigorous stirring, resulting in immediate HCl gas emission. The reaction mixture turned red. After 5 min, a second portion of 67 mg (0.5 mmol) of AlCl3 were added. After 5 min of vigorous stirring, the reaction mixture became hard. After about 1 h, the hard mass obtained was recrystallised from about 100 mL of hot isopropanol. The crystalline product precipitated from this solution at a temperature of −30° C. after a period of time of about 2 to 3 h. It was separated, washed with 50 ml of cold isopropanol, and dried in vacuum under a reduced pressure of 10 to 20 mm Hg. 19.6 g of product were obtained with a yield of 70%. The procedure was repeated with a yield ranging between 67 and 74%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288602B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-377677bcec97417daa5609c25ab5e12c |
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| Source note | uspto-grants-2012_10 |
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