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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452647Generated: October 25, 2026

4-(Trifluoromethoxy)phenylboronic acid → Methyl 3-[4-(trifluoromethoxy)phenyl]-1-benzofuran-5-carboxylate

https://huagongshe.com/reaction/452647

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethoxy)phenylboronic acidHCID 2734386—
ReactantMethyl 3-bromo-1-benzofuran-5-carboxylateHCID 22481688—
ProductMethyl 3-[4-(trifluoromethoxy)phenyl]-1-benzofuran-5-carboxylateHCID 6866436974%

Reaction Steps

In the same manner as in Reference Example 19 and using methyl 3-bromo-1-benzofuran-5-carboxylate instead of methyl 3-iodoimidazo[1,2-a]pyridine-6-carboxylate and [4-(trifluoromethoxy)phenyl]boronic acid instead of (4-methoxyphenyl)boronic acid, the title compound (yield 74%) was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-012678595a654270b42c874153b9326b
Source noteuspto-grants-2013_07