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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51171Generated: October 23, 2026

Methanol → 1-(2-Penten-1-yl)-2-naphthol

https://huagongshe.com/en/reaction/51171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantCyclopentadieneHCID 7612—
ReactantTetrahydrofuranHCID 8028—
Reactant2-NaphtholHCID 8663—
SolventMethyl Isobutyl KetoneHCID 7909—
Product1-(2-Penten-1-yl)-2-naphtholHCID 69887238—

Reaction Steps

Into a 2-liter flask having a stirrer, a condenser and a thermometer, 144 g of 2-naphthol, 200 g of methanol and 40 g of PTS were introduced, and a solution of mixture of 66 g of cyclopentadiene and 60 g of methanol was added dropwise over a period of 3 hours while stirring the mixture at room temperature, followed by further stirring for 4 hours at room temperature. To the reaction solution thus obtained, THF and MIBK were added, and the resultant solution was washed with 200 ml of an aqueous 10% sodium hydroxide solution five times, and thereafter further washed with water until it turned neutral, followed by removal of the solvent using an evaporator. The results of analysis by GPC thereof are shown in FIG. 11. Its yield determined by GPC was 90% (area ratio). An NMR spectrum of the 1-(2-penten-1-yl)-2-naphthol obtained is shown in FIG. 12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713589B2
Source datasetuspto-grants-2004_03
ORD IDord-6f961dfb283f4d78b6133c6ade4457f0
Source noteuspto-grants-2004_03