HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → p-(Cyclopropylmethoxy)-phenoxymethyloxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Cyclopropylmethoxy)phenol | HCID 13755495 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | p-(Cyclopropylmethoxy)-phenoxymethyloxirane | HCID 20223083 | — |
Reaction Steps
A mixture of 0.46 g of sodium hydroxide in 1.8 ml water and 14 ml ethanol, 1.64 g of p-(cyclopropylmethoxy)-phenol and 5.54 g of epichlorohydrin is stirred at room temperature in a nitrogen atmosphere for 24 hours and left at room temperature for 21/2 days. The solvent is evaporated in vacuo and the residue is taken up in ether, washed with water and sodium chloride solution. After drying over anhydrous magnesium sulfate, the solution is filtered and concentrated under reduced pressure to yield p-(cyclopropylmethoxy)-phenoxymethyloxirane which is used directly in the condensation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04634713 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-f6a8206da3214321ba6eea67393d9053 |
| Source note | uspto-grants-1987_01 |