Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277634Generated: October 26, 2026

Formamide → Ethyl alpha-(p-phenoxyphenoxy)alpha-cyclohexylacetate

https://huagongshe.com/reaction/1277634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
Reactant4-PhenoxyphenolHCID 13254—
ReactantEthyl 2-bromo-2-cyclohexylacetateHCID 2762757—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductEthyl alpha-(p-phenoxyphenoxy)alpha-cyclohexylacetateHCID 1302096244.4%

Reaction Steps

Into 15 ml of anhydrous ethanol, 205 mg (0.0089 mole) of methallic sodium was dissolved and then, 1.8 g (0.0089 mole) of p-phenoxyphenol was added. The mixture was stirred at room temperature for about 30 minutes. Ethanol was distilled off under a reduced pressure and 5 ml of dimethyl formamide was added to the residue and dimethyl formamide was distilled off under a reduced pressure and then, 15 ml of dimethyl formamide was added to the residue to dissolve it. Into the solution, 2.5 g (0.010 mole) of ethyl α-bromo-α-cyclohexylacetate was added. The mixture was refluxed for 8 hours and then diemethyl formamide was distilled off under a reduced pressure. The residue was admixed with 50 ml of water and extracted twice with 50 ml of benzene. The benzene layers were combined and washed three times with 30 ml of 5% NaOH aq.sol. and then with water and dehydrated over sodium sulfate and distilled in vacuum to obtain 1.4 g of ethyl α-(p-phenoxyphenoxy)α-cyclohexylacetate (yield: 42.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04278678
Source datasetuspto-grants-1981_07
ORD IDord-bad90d2ee41f474eb5c9a0e5ba89d250
Source noteuspto-grants-1981_07