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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547069Generated: October 30, 2026

Sodium Hydroxide → [5-(4-{1-[4-(3,3-dimethyl-2-oxo-butoxy)-3-methyl-phenyl]-1-ethyl-propyl}-phenyl)-pyridin-3-yl]-acetic Acid

https://huagongshe.com/reaction/547069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
Reactant[5-(4-{1-[4-(3,3-Dimethyl-2-oxo-butoxy)-3-methyl-phenyl]-1-ethylpropyl}-phenyl)-pyridin-3-yl]-acetic acid methyl esterHCID 57709068—
SolventMeOH tetrahydrofuranHCID 21899815—
Product[5-(4-{1-[4-(3,3-dimethyl-2-oxo-butoxy)-3-methyl-phenyl]-1-ethyl-propyl}-phenyl)-pyridin-3-yl]-acetic AcidHCID 5770893967%

Reaction Steps

A 1 N sodium hydroxide aqueous solution (0.182 mL, 0.182 mmol) was added to a solution of [5-(4-{1-[4-(3,3-dimethyl-2-oxo-butoxy)-3-methyl-phenyl]-1-ethylpropyl}-phenyl)-pyridin-3-yl]-acetic acid methyl ester (Example 143-(5); 30.4 mg, 0.061 mmol) in methanol-tetrahydrofuran (1:1, 4 mL), and the mixture was stirred at room temperature for three days. The reaction mixture was then poured into a saturated aqueous ammonium chloride solution, followed by extraction with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (chloroform:methanol=10:1) to give the target compound as a colorless oil (19.8 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935688B2
Source datasetuspto-grants-2011_05
ORD IDord-c2a0fc4dc6b4453cbe5538a1ed0d0e81
Source noteuspto-grants-2011_05