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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603941Generated: November 1, 2026

1-Bromopentane → HCID 53788979, compound

https://huagongshe.com/reaction/1603941

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopentaneHCID 8057—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant4-Methoxy-3-(2-phenylethoxy)benzaldehydeHCID 21716381—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 53788979HCID 53788979—

Reaction Steps

To a suspension of 60% sodium hydride (oily)(0.847 mg) in 25 ml of 1,2-dimethoxyethane, 4.20 ml of triethyl phosphonoacetate was added dropwise over 10 minutes and stirred at room temperature for 1 hour. To this reaction solution, 2.65 ml of pentyl bromide was added, and then refluxed by heating for 3 hours under stirring. Thereafter, the reaction solution was cooled to room temperature and 0.857 mg of 60% sodium hydride (oily) was added thereto. After stirring at room temperature for 30 minutes, 5.15 g of 4-methoxy-3-(2-phenylethoxy)-benzaldehyde was added and refluxed by heating for 2 hours under stirring. Then, the reaction solution was cooled to room temperature, and ethyl acetate and water was added thereto to separate the solution into layers. The organic layer separated was washed with water, an aqueous solution of saturated sodium hydrogencarbonate and a saturated aqueous solution of NaCl in consecutive order and dried over anhydrous magnesium sulfate. The drying agent was separated by filtration, and then the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=30:1) to thereby obtain 5.39 g of ethyl 3-[4-methoxy-3-(2-phenylethoxy)phenyl]-2-pentylacrylate as a mixture of E- and Z-isomers (E-isomer:Z-isomer=7.0:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990151
Source datasetuspto-grants-1999_11
ORD IDord-2df366128e7f487ab7cbc4649cd2ee85
Source noteuspto-grants-1999_11