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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206826Generated: November 1, 2026

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

https://huagongshe.com/reaction/2206826

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 numberUS09373792B2
Source datasetuspto-grants-2016_06
ORD IDord-6e4171fe00584063a3f75b9a4947aab6
Source noteuspto-grants-2016_06