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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617300Generated: October 25, 2026

Water → 2-(5-Tert-butyl-2-hydroxy-4-nitrophenyl)-2-methylpropanoic acid

https://huagongshe.com/reaction/1617300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-(1-Amino-2-methyl-1-oxopropan-2-yl)-4-tert-butyl-5-nitrophenyl methyl carbonateHCID 59544163—
SolventMethanolHCID 887—
Product2-(5-Tert-butyl-2-hydroxy-4-nitrophenyl)-2-methylpropanoic acidHCID 59544150—

Reaction Steps

To a mixture of compound 17 (7.3 g, 21.6 mmol) in methanol (180 mL) was added water (18 mL) and NaOH (8.64 g, 216 mmol). The solution was heated and maintained at reflux for 3 days. The solvent was evaporated in vacuo and the residue was dissolved in 140 mL of water. Then the solution was acidified to pH 2 by the addition of 2N HCl. The aqueous phase was extracted with ethyl acetate (100 mL×3), and the combined organic phases were washed with water and brine, dried over anhydrous Na2SO4 and then concentrated to give compound 18 as a yellow solid, which was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765957B2
Source datasetuspto-grants-2014_07
ORD IDord-254045f9631d4a86930cc94d5cad58a5
Source noteuspto-grants-2014_07