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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589451Generated: November 2, 2026

Ethylene Glycol → Benzoic acid, 4-((1,1-dimethyl-2-((3-phenoxyphenyl)methoxy)ethyl))-, ethyl ester

https://huagongshe.com/reaction/1589451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzonitrile, 4-(1,1-dimethyl-2-((3-phenoxyphenyl)methoxy)ethyl)-HCID 3067160—
SolventWaterHCID 962—
ProductBenzoic acid, 4-((1,1-dimethyl-2-((3-phenoxyphenyl)methoxy)ethyl))-, ethyl esterHCID 3067190—
ProductHCID 20247009HCID 20247009—

Reaction Conditions

Temperature130 °C

Reaction Steps

3-Phenoxybenzyl 2-(4-ethoxycarbonylphenyl)-2-methylpropyl ether was synthesized according to the following procedures. (1) A mixture of 3.5 g of 3-phenoxybenzyl 2-(4-cyanophenyl)-2-methylpropyl ether, 7.0 g of potassium hydroxide, 7.0 g of water and 20 ml of ethylene glycol was stirred at 130° C. for 4.0 hours. The mixture was cooled to room temperature, and water was added and the mixture was made acidic by addition of hydrochloric acid. Then, the mixture was extracted with ether, and the ether extract was washed with water, dried over Na2SO4, and evaporated to give 3.1 g of 3-phenoxybenzyl 2-(carboxyphenyl)-2-methylpropyl ether (mp. 98.5°-102.5° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04570005
Source datasetuspto-grants-1986_02
ORD IDord-77aed698fbbc4a7ba018b146803b30fc
Source noteuspto-grants-1986_02