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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266839Generated: October 29, 2026

4-(2'-Methoxy-biphenyl-4-yloxymethyl)-5-methyl-furan-2-carboxylic acid methyl ester → 4-(2'-Methoxy-biphenyl-4-yloxymethyl)-5-methyl-furan-2-carboxylic acid

https://huagongshe.com/reaction/2266839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2'-Methoxy-biphenyl-4-yloxymethyl)-5-methyl-furan-2-carboxylic acid methyl esterHCID 58824158—
SolventTetrahydrofuranHCID 8028—
Product4-(2'-Methoxy-biphenyl-4-yloxymethyl)-5-methyl-furan-2-carboxylic acidHCID 1844454877.9%

Reaction Steps

A solution of 4-(2′-methoxy-biphenyl-4-yloxymethyl)-5-methyl-furan-2-carboxylic acid methyl ester (125) (40 mg, 0.11 mmoles) in dry tetrahydrofuran (25 ml) was treated with potassium trimethylsilanoate (73 mg, 0.56 mmoles) and the mixture stirred under an argon atmosphere for 16 h. After evaporation of the solvent the residue was acidified to pH=2 with 0.1M aqueous hydrochloric acid and the mixture extracted with ethyl acetate. The dried extracts were evaporated and the residue pumped under high vacuum at 40° C. to afford compound 126 (29 mg) as an off-white solid. LC/MS System D; Rt=8.30 mins, m/z (ES+)=339 (M+H for C20H18O5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858644B2
Source datasetuspto-grants-2010_12
ORD IDord-cf0084176c754b83a25ae6f22a7d87be
Source noteuspto-grants-2010_12