HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → 1-chloro-3-(3-phenyl-3,4-dihydro-2H-1-benzopyrane-7-yloxy)-2-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-Phenylchroman-7-ol | HCID 20496761 | — |
| Product | 1-chloro-3-(3-phenyl-3,4-dihydro-2H-1-benzopyrane-7-yloxy)-2-propanol | HCID 20496716 | — |
Reaction Steps
11.3 g 3-phenyl-7-hydroxy-3,4-dihydro-2H-1-benzopyrane, 0.1 cm3 piperidine and 22 cm3 1-chloro-2,3-epoxypropane were stirred at 90° C. for 9 hours. The solution was evaporated under reduced pressure, then twice 60-60 cm3 of benzene were distilled off from the residue, it was dissolved in 50 cm3 of tetrahydrofurane and into the solution hydrochloric gas was introduced for 5 minutes. The solution was evaporated after an hour's standing, and the residue was crystallized from aceton. 10 g 1-chloro-3-(3-phenyl-3,4-dihydro-2H-1-benzopyrane-7-yloxy)-2-propanol (m.p. 74°-76° C.) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04391821 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-ec6ad1fd9ef4443daf9922b0787e6ae4 |
| Source note | uspto-grants-1983_07 |