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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089293Generated: October 25, 2026

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

https://huagongshe.com/reaction/1089293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium borohydrideHCID 4148881—
ReactantNaphtho[1,2-b]furan-2-carboxylic acid, ethyl esterHCID 14555901—
SolventWaterHCID 962—
ProductNaphtho[1,2-b]furan-2-methanolHCID 1455590285%

Reaction Steps

To a RB flask equipped with magnetic stirring bar, reflux condenser, N2 inlet line with bubbler was added ethyl naphtho[1,2-b]furan-2-carboxylate (H. G. Pars Pharmaceutical Laboratories, Inc., 6.85 g, 28.5 mmol), lithium borohydride (Aldrich, 0.62 g, 28.5 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 (500 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 (80°) to give a total of 4.8 g (69.7%) of naphtho[1,2-b]furan-2-methanol, mp 105.5°-107°, (C,H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04965285
Source datasetuspto-grants-1990_10
ORD IDord-e84ffd0aad8344b18f4b1006cbfb66cb
Source noteuspto-grants-1990_10