HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → HCID 73183747, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 54527042 | HCID 54527042 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 73183747 | HCID 73183747 | — |
Reaction Steps
A mixture of 5.8 g of the product of Step A, 120 ml of acetone, 3.6 g of potassium carbonate and 9.6 ml of epichlorhydrin was refluxed for 24 hours with stirring under an inert atmosphere. Then, 9.6 ml of epichlorhydrin were added and reflux was continued for 5 hours. After filtering, the solvent was evaporated under reduced pressure at 60° C., and the fractions with Rf=0.35 were recovered by chromatography on silica (eluent:methylene chloride) to obtain 5.25 g of 4-[2-[4-[(2-oxiranyl)-methoxy]-phenyl]-ethenyl]-1H-indole melting at ≃128° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04650811 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-2c9facddf2b1480db53320bec3e5f01f |
| Source note | uspto-grants-1987_03 |