HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → 6-Chloro-7-(2,3-epoxypropoxy)-3,4-dihydrocarbostyril
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Chloro-7-hydroxy-3,4-dihydrocarbostyril | HCID 12899420 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Chloro-7-(2,3-epoxypropoxy)-3,4-dihydrocarbostyril | HCID 12899437 | — |
Reaction Steps
20.0 grams of 6-chloro-7-hydroxy-3,4-dihydrocarbostyril and 3.7 g of sodium hydroxide are mixed with 100 ml of methanol and stirred for 3 hours, then 150 ml of epichlorohydrin is added thereto and heated for 5 hours under refluxing conditions. After the reaction is completed, the reaction mixture is concentrated under reduced pressure to dryness. The residue thus obtained is mixed with 100 ml of 2N-sodium hydroxide and stirred well. The insoluble matter is separated by filtration, washed with water and dried. The crude crystals thus obtained are recrystallized from methanol-ethanol to obtain 19.7 g of 6-chloro-7-(2,3-epoxypropoxy)-3,4-dihydrocarbostyril in the form of colorless crystals with a melting point of 190°-192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04824840 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-d807fc37cef644d8b02f38085e388b01 |
| Source note | uspto-grants-1989_04 |