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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345568Generated: October 30, 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/345568

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 1 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 of 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 94).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057525
Source datasetuspto-grants-1991_10
ORD IDord-7e531253a8ec4879a6f0d0c7b585807f
Source noteuspto-grants-1991_10