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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264460Generated: November 1, 2026

Sodium hydride → HCID 178448058, compound

https://huagongshe.com/reaction/1264460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl diethylphosphinoacetateHCID 11788582—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178448068HCID 178448068—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178448058HCID 17844805846.7%

Reaction Conditions

Temperature-5 °C

Reaction Steps

In a flask equipped with a stirrer, a thermometer and a dropping funnel, 3.36 g of sodium hydride was dissolved in 50 ml of THF under nitrogen atmosphere and the solution was cooled down to −5° C. with stirring. 30 ml of a THF solution of ethyl diethylphosphinoacetate (18.8 g) was added dropwise thereto, and the solution was further stirred for 2 hours. After observing hydrogen gas generation, 50 ml of a THF solution of trans-4-(trans-4-propylcyclohexyl)-cyclohexanecarbaldehyde (16.5 g) was added dropwise. Further, the solution was warmed to room temperature and stirred for 3 hours. After stirring, water was added to the reaction mixture and extracted with toluene (50 ml×3). The organic layer was washed with water, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to obtain 10.0 g of ethyl 3-(trans-4-(trans-4-propylcyclohexyl)cyclohexyl)propenoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544604B2
Source datasetuspto-grants-2003_04
ORD IDord-a5528146f7034c4eaf621914d906d00b
Source noteuspto-grants-2003_04