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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993271Generated: October 28, 2026

3-Cyclopentyloxy-4-methoxybenzaldehyde → trans-1-(3-Cyclopentyloxy-4-methoxyphenyl)-2-(2,6-dichlorophenyl)ethene

https://huagongshe.com/reaction/993271

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
Reactant2,6-Dichlorobenzyltriphenylphosphonium bromideHCID 11843551—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Producttrans-1-(3-Cyclopentyloxy-4-methoxyphenyl)-2-(2,6-dichlorophenyl)etheneHCID 2214579364.1%

Reaction Steps

A stirred suspension of 2,6-dichlorobenzyltriphenylphosphonium bromide (2.5 g) in dry tetrahydrofuran (30 mL) is treated dropwise with a solution of potassium t-butoxide (0.56 g) in dry tetrahydrofuran (32 mL) at 0° C. After stirring at this temperature for 1 hour, it is treated with a solution of 3-cyclopentyloxy-4-methoxybenzaldehyde (1.1 g) in dry tetrahydrofuran (15 mL). The reaction mixture is stirred from 0° C. to 5° C. for 1.5 hours, and then allowed to warm to room temperature. After stirring overnight, the mixture is concentrated and the resulting residue is treated with ethyl acetate (200 mL). The resulting organic solution is filtered. The filtrate is concentrated and the resulting residue is subjected to flash chromatography, eluting with dichloromethane, to give trans-1-(3-cyclopentyloxy-4-methoxyphenyl)-2-(2,6-dichlorophenyl)ethene (1.16 g), m.p. 47-49° C. [Elemental analysis: C, 66.4; H, 5.6; Cl, 19.4%, calculated: C, 66.1; H, 5.55; Cl, 19.5%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06472412B1
Source datasetuspto-grants-2002_10
ORD IDord-03d8148a480a45bd84be525aedb096e4
Source noteuspto-grants-2002_10