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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051252Generated: October 27, 2026

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

https://huagongshe.com/reaction/2051252

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 numberUS05017600
Source datasetuspto-grants-1991_05
ORD IDord-bfec2c34c10a4f9085b1a8860414b092
Source noteuspto-grants-1991_05