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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613930Generated: November 2, 2026

Hydrochloric Acid → 2-(2-Biphenyl-4-yl-furan-5-yl)-acetic acid

https://huagongshe.com/reaction/613930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
Reactant2-(2-Biphenyl-4-yl-furan-5-yl)-acetic acid ethyl esterHCID 18341510—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Biphenyl-4-yl-furan-5-yl)-acetic acidHCID 18380301100%

Reaction Steps

To a solution of 2-(2-biphenyl-4-yl-furan-5-yl)-acetic acid ethyl ester (0.465 g, 1.44 mmol) in THF (10 mL) at 0° C. was added 2M aqueous LiOH (2 mL). The mixture was allowed to warm over 4 hours to ambient temperature and then poured into 0.5M aqueous HCl (50 mL). The resultant pale orange precipitate was filtered off, rinsed with water, and dried under vacuum over P2O5 to provide 400 mg (100%) of 2-(2-biphenyl-4-yl-furan-5-yl)-acetic acid as a light orange solid, mp 196-210° C., used without further purification. 1H NMR (acetone-d6): δ 7.78 (d, 2H, J=8.1 Hz), 7.72-7.67 (m, 4H), 7.46 (t, 2H, J=7.4 Hz), 7.35 (t, 1H, J=7.4 Hz), 6.84 (d, 1H, J=3.3 Hz), 6.41 (d, 1H, J=3.3 Hz), 3.81 (s, 2H). Anal. Calculated for C18H14O3 : C, 77.68; H, 5.07. Found: C, 77.44; H, 5.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008243
Source datasetuspto-grants-1999_12
ORD IDord-55fb6bccc65b4f3f932b55d89dc79408
Source noteuspto-grants-1999_12