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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280684Generated: October 30, 2026

Water → 2-((S)-6-((2'-(hydroxymethyl)-6'-methyl-4'-(((R)-tetrahydrofuran-3-yl)oxy)biphenyl-3-yl)methoxy)-2,3-dihydrobenzofuran-3-yl)acetic acid

https://huagongshe.com/reaction/2280684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 2-((S)-6-((2'-(acetoxymethyl)-6'-methyl-4'-(((R)-tetrahydrofuran-3-yl)oxy)biphenyl-3-yl)methoxy)-2,3-dihydrobenzofuran-3-yl)acetateHCID 89701761—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-((S)-6-((2'-(hydroxymethyl)-6'-methyl-4'-(((R)-tetrahydrofuran-3-yl)oxy)biphenyl-3-yl)methoxy)-2,3-dihydrobenzofuran-3-yl)acetic acidHCID 897017568.6%

Reaction Steps

The crude methyl 2-((S)-6-((2′-(acetoxymethyl)-6′-methyl-4′-(((R)-tetrahydrofuran-3-yl)oxy)biphenyl-3-yl)methoxy)-2,3-dihydrobenzofuran-3-yl)acetate 35e (189 mg, 0.36 mmol) was dissolved in 10 mL of a mixture of the solvents of methanol and tetrahydrofuran (V/V=1:4), followed by addition of 1M aqueous lithium hydroxide solution (4 mL, 4 mmol). The reaction solution was stirred for 3 hours. The resulting solution was added with 50 mL of water and 5 mL of 2M aqueous sodium hydroxide solution. The aqueous phase was washed with ethyl acetate (30 mL), then 1M hydrochloric acid was added dropwise to adjust the pH to 2-3, and 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 and the residue was purified by TLC with elution system A to obtain the title compound 2-((S)-6-((2′-(hydroxymethyl)-6′-methyl-4′-(((R)-tetrahydrofuran-3-yl)oxy)biphenyl-3-yl)methoxy)-2,3-dihydrobenzofuran-3-yl)acetic acid 35 (15 mg, yield 8.6%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139548B2
Source datasetuspto-grants-2015_09
ORD IDord-495cdb8303314d02ab382772a8600a4c
Source noteuspto-grants-2015_09