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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165646Generated: October 25, 2026

Hydrochloric Acid → Phenanthro[1,2-b]furan-2-methanol

https://huagongshe.com/reaction/1165646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium borohydrideHCID 4148881—
ReactantEthyl phenanthro(1,2-b]furan-2-carboxylateHCID 12274414—
SolventWaterHCID 962—
ProductPhenanthro[1,2-b]furan-2-methanolHCID 1477023990.3%

Reaction Steps

To a RB flask equipped with magnetic stirring bar, reflux condenser and N2 inlet tube with bubbler was added ethyl phenanthro[1,2-b]furan-2-carboxylate (H. G. Pars Pharmaceutical Laboratories, Inc., 7.9 g, 27.2 mmol), lithium borohydride (Aldrich, 0.65 g, 30 mmol) and dry THF (400 mL). The mixture was stirred at reflux for 6 h and then poured into H2O (1 L). The reaction mixture was acidified with 1N HCl and the resulting white solid was filtered, washed with additional H2O (1500 mL) then dissolved in CH2Cl2 (500 mL), dried (Na2SO4), filtered, concentrated to 200 mL and diluted to 500 mL with hexane. The resulting material was filtered, washed with hexane (100 mL) and placed in a vacuum oven overnight. A total of 6.1 g (90.1%) of phenanthro[1,2-b]-furan-2-methanol, mp 125°-126° was obtained (C,H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04910218
Source datasetuspto-grants-1990_03
ORD IDord-abb1e924a370437bba764777d23bab25
Source noteuspto-grants-1990_03