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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177334Generated: October 30, 2026

Ethyl 3-(2,3-difluoro-4-hydroxyphenyl)propanoate → HCID 85473101, compound

https://huagongshe.com/reaction/2177334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(2,3-difluoro-4-hydroxyphenyl)propanoateHCID 90404786—
ReactantHCID 90418025HCID 90418025—
ReactantHCID 90418246HCID 90418246—
ProductHCID 85473101HCID 85473101—

Reaction Steps

The title compound was prepared according to the procedure described in Example 196 by coupling of [5-chloro-3-(4-ethylphenyl)thiophen-2-yl]methanol and ethyl 3-(4-hydroxy-2,3-difluorophenyl)propanoate followed by hydrolysis of ethyl 3-(4-((5-chloro-3-(4-chlorophenyl)thiophen-2-yl)methoxy)-2,3-difluorophenyl)propanoate to afford the desired product as an off-white solid. 1H NMR (400 MHz, CDCl3) 7.26-7.33 (m, 4H), 6.95 (s, 2H), 6.85 (t, J=8.8 Hz, 2H), 6.59-6.64 (t, J=8.4 Hz, 1H), 6.62 (t, J=8.4 Hz, 1H), 5.13 (s, 2H), 2.96 (t, J=7.8 Hz, 2H), 2.67-2.74 (m, 4H), 1.29 (t, J=7.6 Hz, 3H). Mass spectrum (ESI, m/z): Calcd. for C22H19ClF2O3S, 435.1 (M−H). found 435.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-ac8634443a504b1db3af408fd6e24a3b
Source noteuspto-grants-2015_06