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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177341Generated: October 30, 2026

Ethyl 3-(4-hydroxy-2,3-dimethylphenyl)propanoate → HCID 85472863, compound

https://huagongshe.com/reaction/2177341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(4-hydroxy-2,3-dimethylphenyl)propanoateHCID 58566491—
ReactantHCID 90418810HCID 90418810—
ReactantHCID 90418821HCID 90418821—
ProductHCID 85472863HCID 85472863—

Reaction Steps

The title compound was prepared according to the procedure described in Example 196 by coupling of [3-(4-ethylphenyl)-5-fluorothiophen-2-yl]methanol and ethyl 3-(4-hydroxy-2,3-dimethylphenyl)propanoate followed by hydrolysis of ethyl 3-(4-((5-fluoro-3-(4-ehtylphenyl)thiophen-2-yl)methoxy)-2,3-dimethylphenyl)propanoate to afford the desired product as an off-white solid. 1H-NMR (300 MHz, CD3OD) δ 7.34 (d, J=8.1 Hz, 2H), 7.26 (d, J=8.1 Hz, 2H), 6.92 (d, J=8.4 Hz, 2H), 6.62-6.64 (m, 2H), 5.05 (s, 2H), 2.89 (t, J=8.1 Hz, 2H), 2.65-2.72 (m, 2H), 2.49 (d, J=8.1 Hz, 2H), 2.24 (s, 3H), 2.21 (s, 3H), 1.29 (t, J=7.5 Hz, 3H). Mass spectrum (ESI, m/z): Calcd. for C24H25FO3S, 411.2 (M−H). found 411.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-d74a08fc52d34f55b872bd9ea6bb4528
Source noteuspto-grants-2015_06