HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756889Generated: October 28, 2026
Water → (2,4-Bis(1,1-dimethylpropyl)phenoxy)acetic acid
https://huagongshe.com/reaction/1756889
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl [2,4-bis(2-methylbutan-2-yl)phenoxy]acetate | HCID 19391876 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (2,4-Bis(1,1-dimethylpropyl)phenoxy)acetic acid | HCID 83411 | 133.8% |
Reaction Steps
The above ethyl 2-(2,4-di-t-amylphenoxy)acetate (293 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 (289.5 g) was added thereto, followed by extraction. The water layer was separated with a separatory funnel, and the toluene layer was washed with water (289.5 g). Then, the toluene layer was concentrated by distillation under ordinary pressure for the recovery 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05442114 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-145f2852474d403f8ef98a103d0fb8c9 |
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| Source note | uspto-grants-1995_08 |
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