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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890880Generated: October 29, 2026

ethyl 3-fluoro-5-(4-methoxy-3,4,5,6-tetrahydro-2H-pyran-4-yl)phenoxyacetate → 3-fluoro-5-(4-methoxy-3,4,5,6-tetrahydro-2H-pyran-4-yl)phenoxyacetic acid

https://huagongshe.com/reaction/890880

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 3-fluoro-5-(4-methoxy-3,4,5,6-tetrahydro-2H-pyran-4-yl)phenoxyacetateHCID 22246123—
SolventCitric AcidHCID 311—
SolventLithium HydroxideHCID 3939—
Product3-fluoro-5-(4-methoxy-3,4,5,6-tetrahydro-2H-pyran-4-yl)phenoxyacetic acidHCID 2224621095%

Reaction Steps

A solution of ethyl 3-fluoro-5-(4-methoxy-3,4,5,6-tetrahydro-2H-pyran-4-yl)phenoxyacetate (Step 1) (0.3 g, 1 mmol) in ethanolic LiOH (1M, 1.5 mL) was stirred at room temperature for 2 h. The reaction mixture was diluted with 5% citric acid (10 mL) and extracted with ether (2×15 mL). The ether extracts were combined and washed with water (2×20 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to give 0.26 g (95%) of 3-fluoro-5-(4-methoxy-3,4,5,6-tetrahydro-2H-pyran-4-yl)phenoxyacetic acid as a colorless viscous liquid: 1H NMR (CDCl3/300 MHz) δ 6.78 (d, 2H, J=10.5 Hz), 6.50 (d, 1H, J=10.5 Hz), 4.68 (s, 2H), 3.82 (m, 4H), 2.99 (s, 3H), 1.92 (m, 4H); FABMS m/z=284 (M+H). HRMS calcd for C14H17FO5 283.0982, found 283.0993.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06998415B2
Source datasetuspto-grants-2006_02
ORD IDord-6262ba12f0734e0c95005c779cfd2498
Source noteuspto-grants-2006_02