Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074455Generated: October 27, 2026

Epichlorohydrin → 1-chloro-3-(3-phenyl-3,4-dihydro-2H-1-benzopyrane-7-yloxy)-2-propanol

https://huagongshe.com/reaction/1074455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantPiperidineHCID 8082—
Reactant3-Phenylchroman-7-olHCID 20496761—
Product1-chloro-3-(3-phenyl-3,4-dihydro-2H-1-benzopyrane-7-yloxy)-2-propanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04391821
Source datasetuspto-grants-1983_07
ORD IDord-ec6ad1fd9ef4443daf9922b0787e6ae4
Source noteuspto-grants-1983_07