HuagongsheHuagongshe Chemistry Print Report · For research reference only
Urea → 4-p-Tolylethynylphenyl 4-vinylcyclohexanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-Ethenylcyclohexane-1-carboxylic acid | HCID 18538169 | — |
| Reactant | 4-[2-(4-Methylphenyl)ethynyl]phenol | HCID 18739027 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-p-Tolylethynylphenyl 4-vinylcyclohexanecarboxylate | HCID 59929138 | — |
Reaction Steps
5.0 g of 4-vinylcyclohexanecarboxylic acid, 6.7 g of 4-p-tolylethynylphenol, 4.0 g of 4-(dimethylamino)pyridine and 250 ml of toluene were mixed at RT, 7.3 g of DCC in 50 ml of toluene were added, and the mixture was stirred vigorously overnight at RT, during which the urea formed precipitated. 1 g of oxalic acid was then added, and the mixture was stirred at RT for a further hour in order to destroy the excess DCC. The conventional work-up gave 4-p-tolylethynylphenyl 4-vinylcyclohexanecarboxylate in the form of colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06171664B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-9c62461c638c4c36b920de2febc79126 |
| Source note | uspto-grants-2001_01 |