Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756890Generated: October 29, 2026

Water → Butanoic acid, 2-[2,4-bis(1,1-dimethylpropyl)phenoxy]-

https://huagongshe.com/reaction/1756890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-[2,4-bis(2-methylbutan-2-yl)phenoxy]butanoateHCID 19391871—
SolventTolueneHCID 1140—
ProductButanoic acid, 2-[2,4-bis(1,1-dimethylpropyl)phenoxy]-HCID 625983122.3%

Reaction Steps

The above ethyl 2-(2,4-di-t-amylphenoxy)butyrate (317.9 g) and 27% aqueous sodium hydroxide (401.4 g) were placed in a 3-liter flask. The mixture was kept at 98° C. for 6 hours, and the hydrolysis reaction was completed. After completion of the reaction, the mixture was adjusted to pH 2 or lower by the addition of 40% aqueous sulfuric acid (349.9 g) and water (250 g), and toluene (317.9 g) was added thereto, followed by extraction. The water layer was separated with a separatory funnel, and the toluene layer was washed with water (317.9 g). Then, the toluene layer was concentrated by distillation under ordinary pressure for the removal of toluene, which afforded a concentrated solution (357.6 g) of the carboxylic acid compound in toluene. The analysis revealed that the concentrated solution contained the desired carboxylic acid compound in a yield of 99% on the basis of the raw material ester compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05442114
Source datasetuspto-grants-1995_08
ORD IDord-fe65d43e86444eecaf8d708634fbde03
Source noteuspto-grants-1995_08