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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35304Generated: October 29, 2026

1-(4-fluorophenyl)-1,3-dihydro-1-[3-(tetrahydro-2H-pyran-2-yloxy)propyl]isobenzofuran → 1-(4-Fluorophenyl)-1,3-dihydroisobenzofuran-1-propanol

https://huagongshe.com/reaction/35304

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-fluorophenyl)-1,3-dihydro-1-[3-(tetrahydro-2H-pyran-2-yloxy)propyl]isobenzofuranHCID 19883543—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product1-(4-Fluorophenyl)-1,3-dihydroisobenzofuran-1-propanolHCID 19883527—

Reaction Steps

39.6 Parts of 1-(4-fluorophenyl)-1,3-dihydro-1-[3-(tetrahydro-2H-pyran-2-yloxy)propyl]isobenzofuran were dissolved in 9.8 parts of a hydrochloric acid solution 0.1M and 788 parts of ethanol and the whole was stirred and refluxed for one hour. The solvent was evaporated and the residue was taken up in methylbenzene and water. The organic phase was separated, washed with water, dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using a mixture trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 24.2 parts of 1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-1-propanol as a residue (intermediate 11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766125
Source datasetuspto-grants-1988_08
ORD IDord-67e67dd8dc1c49ee9eca8cd4fd777ddb
Source noteuspto-grants-1988_08