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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175612Generated: October 25, 2026

4-Methyl-3-thiopheneboronic acid → Ethyl 2-(3-methoxy-4-(4-methylthiophen-3-yl)phenyl)acetate

https://huagongshe.com/reaction/1175612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-3-thiopheneboronic acidHCID 5083931—
ReactantEthyl (3-methoxy-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)acetateHCID 58820079—
ProductEthyl 2-(3-methoxy-4-(4-methylthiophen-3-yl)phenyl)acetateHCID 6877542872%

Reaction Steps

Prepared in a similar manner to example 1 from ethyl 2-(3-methoxy-4-(trifluoromethylsulfonyloxy)phenyl)acetate (example 27d) and 4-methylthiophen-3-ylboronic acid. Yield: 72%. 1H NMR (400 MHz, dMSO): δ 1.19-1.22 (m, 3H), 2.00 (s, 3H), 3.62 (s, 2H), 3.69-3.73 (m, 3H), 4.08-4.13 (m, 2H), 6.86-6.88 (d, 1H), 6.98-6.99 (d, 1H), 7.08-7.10 (d, 1H), 7.16-7.17 (t, 1H), 7.26-7.27 (d,1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842324B2
Source datasetuspto-grants-2010_11
ORD IDord-ad391cb7dfed4f9ebfbd57e4f9441513
Source noteuspto-grants-2010_11