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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035708Generated: October 31, 2026

Sodium hydride → HCID 178468870, compound

https://huagongshe.com/reaction/1035708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantPotassium bisulfateHCID 516920—
Reactanttert-Butyl diethylphosphonoacetateHCID 2773685—
ReactantHCID 178468872HCID 178468872—
SolventDimethylformamideHCID 6228—
ProductHCID 178468870HCID 17846887080.5%

Reaction Steps

0.682 g of tert-butyl diethylphosphonoacetate (2.7 mmol, 1.1 eq.) is placed in 5 mL of DMF at 4° C. with stirring, 0.065 g of sodium hydride (2.7 mmol, 1.1 eq.) is added. After stirring for 1 hour, 0.64 g of ethyl trans-4-(4-formylcyclohexyl)benzoate (2.46 mmol, 1 eq.) dissolved in 5 mL of DMF is added dropwise. After stirring for 18 hours, 10% potassium hydrogen sulfate solution is added. The reaction medium is extracted twice with ethyl acetate. The organic phases are combined, washed twice with water, washed with brine, dried over sodium sulfate and evaporated. The residue is chromatographed on silica gel with a gradient of ethyl acetate in heptane ranging from 10% to 20%. 0.71 g of ethyl trans-4-[4-((E)-2-tert-butoxycarbonylvinyl)cyclohexyl]benzoate is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546391B2
Source datasetuspto-grants-2013_10
ORD IDord-737ff7aed4df4910bdf67333ac419e00
Source noteuspto-grants-2013_10