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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383512Generated: October 26, 2026

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

https://huagongshe.com/reaction/1383512

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 numberUS06255326B1
Source datasetuspto-grants-2001_07
ORD IDord-7535f25d677a4f3491eaf03500c12a1b
Source noteuspto-grants-2001_07