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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470727Generated: October 30, 2026

1-Naphthol → 7,8,9,10-Tetrahydrobenzo[b]naphtho[2,1-d]furan

https://huagongshe.com/reaction/470727

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphtholHCID 7005—
Reactant1,3-CyclohexadieneHCID 11605—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTolueneHCID 1140—
Product7,8,9,10-Tetrahydrobenzo[b]naphtho[2,1-d]furanHCID 26855525%

Reaction Steps

144 g of 1-naphthol, 190 g of p-toluenesulfonic acid monohydrate, 80.1 g of 1,3-cyclohexadiene and 4 L of toluene were placed in a flask. The resulting mixture was stirred under reflux for 24 hours. After cooling to room temperature, the reaction solution was washed with 600 mL of water. After drying an organic phase with magnesium sulfate, the solvent was distilled off under reduced pressure. Residues were purified by silica gel column chromatography, whereby 55.5 g (yield: 25%) of 7,8,9,10-tetrahydrobenzo[b]naphtho[2,1-d]furan was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629430B2
Source datasetuspto-grants-2014_01
ORD IDord-272f4450c6e64cd1a060c609e02625cb
Source noteuspto-grants-2014_01