HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530154Generated: October 26, 2026
2-Chloroethyl vinyl ether → 1-Cyclohexyl-4-[2-(ethenyloxy)ethoxy]benzene
https://huagongshe.com/reaction/1530154
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethyl vinyl ether | HCID 8074 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Cyclohexylphenol | HCID 14327 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Cyclohexyl-4-[2-(ethenyloxy)ethoxy]benzene | HCID 22011687 | — |
Reaction Steps
p-Cyclohexylphenol (83.1 g (0.5 mol)) was dissolved in 300 ml of toluene, and 150 g of 2-chloroethyl vinyl ether was added thereto. Furthermore, 25 g of sodium hydroxide, 5 g of tetrabutylammonium bromide and 60 g of triethylamine were added, and the resulting mixture was heated with stirring at 120° C. for 5 hours. The reaction solution was washed with water, and excess chloroethyl vinyl ether and toluene were removed by distillation under reduced pressure. From the obtained oil, the objective p-cyclohexylphenoxyethyl vinyl ether (X-1) was obtained by distillation under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09090722B2 |
|---|
| Source dataset | uspto-grants-2015_07 |
|---|
| ORD ID | ord-9a25d57c76dd446f8ce17c907f969ed5 |
|---|
| Source note | uspto-grants-2015_07 |
|---|