HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841132Generated: October 30, 2026
Water → Tert-butyl 4'-methylbiphenyl-2-carboxylate
https://huagongshe.com/reaction/841132
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-(4-Methylphenyl)benzoic acid | HCID 81568 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl 4'-methylbiphenyl-2-carboxylate | HCID 9838270 | 95.7% |
Reaction Steps
A 500-ml flask was charged with 50 ml of toluene and 53.42 g (0.25 mol) of 4′-methyl-2-biphenylcarboxylic acid, 0.45 ml (0.025 mol) of water and 32.63 g (0.58 mol) of isobutene. To this mixture was added dropwise 7.74 g (0.05 mol) of phosphorus oxytrichloride, and the mixture was stirred for 6 hours. The reaction mixture was added to 50 ml of a 10%-aqueous sodium hydroxide and washed. The organic layer was dried over anhydrous magnesium sulfate. Thereafter, the organic layer was concentrated by distilling off toluene by using a rotary evaporator, to give 64.2 g of tert-butyl 4′-methyl-2-biphenylcarboxylate as crystals (yield: 95% based on 4′-methyl-2-biphenylcarboxylic acid, purity by HPLC: 99.9%). Incidentally, the obtained compound had the same physical properties as those of the compound obtained in Example II-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06369266B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-6ec4bd531d3840cc9bddfb117ceba82e |
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| Source note | uspto-grants-2002_04 |
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