Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131157Generated: October 26, 2026

Hydrochloric Acid → 4-(3-Hydroxypropyl)benzene-1,3-diol

https://huagongshe.com/reaction/131157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium borohydrideHCID 4148881—
ReactantUmbelliferoneHCID 5281426—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Hydroxypropyl)benzene-1,3-diolHCID 1295840342%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a stirred solution of 7-hydroxycoumarin (7.0 g, 43.2 mmol ) in anhydrous THF (200 mL ) at rt under argon was added Lithium borohydride (2M, 65.8 mL, 129.6 mmol, 3.0 eq) solution in THF dropwise. Anhydrous methanol (1.0 mL) was added as catalyst to the reaction mixture. The mixture was heated at 65° C. for 17 h. The reaction mixture was then cooled to ambient temperature. Saturated ammonium chloride solution (40 mL) was added dropwise to the solution, followed by 1N HCl solution (40 mL). The mixture was extracted with ethyl acetate (2×100 mL). The combined organic extracts were dried (Na2SO4), filtered, and evaporated in vacuo. The residue was purified on silica gel (flash column chromatography) eluting with 30% ethyl acetate-hexane to provide the desired product as white solid (3.05 g, 42%). 1H-NMR (CD3CN) δ 6.91 (d, 1H), 6.29 (s, 1H), 6.28 (d, 1H), 3.51 (t, 2H), 2.56 (t, 2H), 1.73 (m, 2H). MS GC-MS (M+=168).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384947B2
Source datasetuspto-grants-2008_06
ORD IDord-2fc1d2009a2d44c289d36fbe7124f4df
Source noteuspto-grants-2008_06