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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177356Generated: October 30, 2026

Ethyl 3-(4-hydroxy-2,3-dimethylphenyl)propanoate → HCID 90418407, compound

https://huagongshe.com/reaction/2177356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(4-hydroxy-2,3-dimethylphenyl)propanoateHCID 58566491—
ReactantHCID 90418009HCID 90418009—
ReactantHCID 90418258HCID 90418258—
ProductHCID 90418407HCID 90418407—

Reaction Steps

The title compound was prepared according to the procedure described in Example 208 by coupling of (3-(4-ethylphenyl)-5-(trifluoromethyl)thiophen-2-yl)methanol and ethyl 3-(4-hydroxy-2,3-dimethyl phenyl)propanoate followed by hydrolysis of ethyl 3-(4-((3-(4-ethylphenyl)-5-(trifluoromethyl)thiophen-2-yl)methoxy)-2,3-dimethylphenyl)propanoate to afford the desired product as an off-white solid. 1H NMR (400 MHz, CDCl3) δ 7.46 (s, 1H), 7.35 (d, J=6.0 Hz, 2H), 7.28 (d, J=6.0 Hz, 2H), 6.95 (d, J=5.3 Hz, 1H), 6.65 (d, J=5.3 Hz, 1H), 5.15 (s, 2H), 2.96 (t, J=5.5 Hz, 2H), 2.68 (q, J=5.5 Hz, 2H), 2.60 (t, J=6.0 Hz, 2H), 2.25 (s, 3H), 2.18 (s, 3H), 1.28 (t, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-0f1f05d5cbdb4468bca1d5eccbd0eaa4
Source noteuspto-grants-2015_06