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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219778Generated: October 26, 2026

4-Methyl-3-thiopheneboronic acid → Methyl 3-methoxy-4-(4-methyl-3-thienyl)benzoate

https://huagongshe.com/reaction/219778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-3-thiopheneboronic acidHCID 5083931—
ReactantMethyl 4-bromo-3-methoxybenzoateHCID 14570117—
Reactant3-Methyl-4-[2-(trifluoromethyl)phenyl]benzoic acidHCID 21947812—
ProductMethyl 3-methoxy-4-(4-methyl-3-thienyl)benzoateHCID 67400074—

Reaction Steps

The title compound was prepared following procedure described for Intermediate 5, step 1, but starting from methyl 4-bromo-3-methoxybenzoate (Combi-Blocks, 2.50 g; 10.20 mmol; 1 eq.) and 4-methyl-3-thiopheneboronic acid (1.59 g; 11.22 mmol; 1.10 eq.), and was isolated as a brown oil. It was used in the next step without further purification. LC/MS (Method A): 262.8 (M+H)+. HPLC (Method A) Rt 4.79 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-7d8965b4a54c45388d0ca83d52c83b3c
Source noteuspto-grants-2012_06