HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → 4-Benzyloxy-7-(2,3-epoxypropyloxy)coumarin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Benzyloxy-7-hydroxycoumarin | HCID 13408407 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Benzyloxy-7-(2,3-epoxypropyloxy)coumarin | HCID 13408408 | — |
Reaction Steps
4-Benzyloxy-7-hydroxycoumarin (10.7 g, 0.041 mole) was dissolved in ethanol (200 ml) and a solution of potassium hydroxide (2.5 g) in water (10 ml) was added. Epichlorhydrin (40 ml) was added and the stirred mixture heated to reflux for 21/2 hr. After cooling, the solvent was removed in vacuo and the residue partitioned between water and ethyl acetate. Evaporation of the dried (MgSO4) organic phase gave the product as a white crystalline solid. Recrystallization from ethanol gave 11.1 g (83%) of material of m.p. 128°-129° C.; (Found; C, 70.48; H, 4.92; C19H16O5 requires; C, 70.36; H, 4.97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04263299 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-9d0ac0a5027940a7aa31852e5a9d8c75 |
| Source note | uspto-grants-1981_04 |