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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089006Generated: October 26, 2026

Sodium Hydroxide → 4-(2',3'-Dimethoxyphenyl) 3-phenylbutyric acid

https://huagongshe.com/reaction/1089006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-(2',3'-dimethoxyphenyl)-3-phenylbutyrateHCID 19961164—
SolventMethanolHCID 887—
Product4-(2',3'-Dimethoxyphenyl) 3-phenylbutyric acidHCID 12478543100.2%

Reaction Steps

Ethyl 4-(2',3'-dimethoxyphenyl)-3-phenylbutyrate (40.3 g, 123 mmol), from Step 3, was dissolved in 400 mL of methanol and 62 mL of 3 M aqueous sodium hydroxide solution was added in one portion. The reaction mixture was stirred at ambient temperature for 18 h. The reaction mixture was concentrated and the residue was partitioned between 300 mL of diethyl ether and 200 mL of water. The layers were separated and the aqueous layer was adjusted to pH 6 with 6 M aqueous hydrochloric acid solution and extracted with 3×200 mL of diethyl ether. The organic layers were combined, washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to give 37 g (100% yield) of the title compound as a colorless oil. The 1H NMR spectrum was identical to the spectrum reported for the product of Step 5 of Method A, Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963568
Source datasetuspto-grants-1990_10
ORD IDord-206d20c166084578b16977359d0c3eed
Source noteuspto-grants-1990_10