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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994326Generated: November 3, 2026

3-Chlorocyclopent-1-ene → 3-Cyclopent-2-enyloxy-4-methoxybenzaldehyde

https://huagongshe.com/reaction/1994326

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorocyclopent-1-eneHCID 7297—
ReactantIsovanillinHCID 12127—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product3-Cyclopent-2-enyloxy-4-methoxybenzaldehydeHCID 22145828—

Reaction Steps

A solution of 3-hydroxy-4-methoxybenzaldehyde (14.20 g) in dry dimethylformamide (300 mL) is treated portionwise with sodium hydride (60% dispersion in oil; 3.70 g) at room temperature under nitrogen. 3-Chlorocyclo-pentene (9.6 mL) is added and the resulting mixture is stirred overnight. The solvent is then removed under reduced pressure and the residue is partitioned between water (500 mL) and dichloromethane (500 mL) and the aqueous layer is further extracted with dichloromethane (500 mL). The combined organic extracts are dried and evaporated under reduced pressure and the residue is subjected to flash chromatography on silica gel, eluting with a mixture of ethyl acetate and pentane (1:1 v/v), to give 3-cyclopent-2-enyloxy-4-methoxybenzaldehyde, in the form of a pale brown oil (11.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652144B2
Source datasetuspto-grants-2010_01
ORD IDord-b1e297ad18c44d4bbc31c7a39eb676e1
Source noteuspto-grants-2010_01