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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280628Generated: October 30, 2026

Sodium Hydroxide → 2-((S)-6-((2',6'-dimethyl-4'-(((S)-tetrahydrofuran-3-yl)oxy)biphenyl-3-yl)methoxy)-2,3-dihydrobenzofuran-3-yl)acetic acid

https://huagongshe.com/reaction/2280628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 2-((S)-6-((2',6'-dimethyl-4'-(((S)-tetrahydrofuran-3-yl)oxy)biphenyl-3-yl)methoxy)-2,3-dihydrobenzofuran-3-yl)acetateHCID 89701763—
SolventMethanolHCID 887—
Product2-((S)-6-((2',6'-dimethyl-4'-(((S)-tetrahydrofuran-3-yl)oxy)biphenyl-3-yl)methoxy)-2,3-dihydrobenzofuran-3-yl)acetic acidHCID 71656814100%

Reaction Steps

Methyl 2-((S)-6-((2′,6′-Dimethyl-4′-(((S)-tetrahydrofuran-3-yl)oxy)biphenyl-3-yl)methoxy)-2,3-dihydrobenzofuran-3-yl)acetate 1d (220 mg, 0.45 mmol) was dissolved in 15 mL of methanol, followed by addition of 3 M aqueous sodium hydroxide solution (1.5 mL, 4.50 mmol). The reaction mixture was reacted for 3 hours. The mixture was concentrated under reduced pressure, mixed with 10 mL of water, and 1M hydrochloric acid was added dropwise to adjust the pH to 2. The resulting solution was extracted with ethyl acetate (20 mL×2). The combined organic extracts were washed with saturated sodium chloride solution (30 mL), dried with anhydrous magnesium sulphate, and filtered. The filtrate was concentrated under reduced pressure to obtain the title compound 2-((S)-6-((2′,6′-dimethyl-4′-(((S)-tetrahydrofuran-3-yl)oxy)biphenyl-3-yl)methoxy)-2,3-dihydrobenzofuran-3-yl)acetic acid 1 (210 mg, yield 100%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139548B2
Source datasetuspto-grants-2015_09
ORD IDord-2e6ded9920d9452da9b1d39d8a055df5
Source noteuspto-grants-2015_09