HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → 1-{2-[(Oxiran-2-yl)methoxy]phenyl}-1H-pyrrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(1H-Pyrrol-1-Yl)Phenol | HCID 712334 | — |
| Product | 1-{2-[(Oxiran-2-yl)methoxy]phenyl}-1H-pyrrole | HCID 13755510 | — |
Reaction Steps
95.7 g of o-(pyrrol-1-yl)-phenol, 245 g of potassium carbonate and 167 g of epichlorohydrin are heated to the boil in a nitrogen atmosphere, whilst stirring. After 6 hours, the reaction mixture is cooled and filtered and the filtrate is evaporated in vacuo, ultimately at a bath temperature of 120° C. The oil which remains is dissolved in 300 ml of ether and the solution is extracted with 300 ml of 2 N sodium hydroxide solution and washed with 100 ml of water. The oil which remains after evaporating off the solvent is distilled in a high vacuum and gives 1-[o-(pyrrol-1-yl)-phenoxy]-2,3-epoxy-propane of boiling point 103°-105° C/0.001 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03984436 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-2028f0fe27ac4ef8a1dba9f9bc591004 |
| Source note | uspto-grants-1976_10 |