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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397465Generated: October 29, 2026

3-Carboxyphenylboronic acid → HCID 67323228, compound

https://huagongshe.com/reaction/1397465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Carboxyphenylboronic acidHCID 2733957—
Reactant1-(5-Bromothiophen-3-yl)-2,2,2-trifluoroethan-1-oneHCID 67324122—
ProductHCID 67323228HCID 6732322816%

Reaction Steps

This compound was synthesized from 1-(5-bromothiophen-3-yl)-2,2,2-trifluoroethanone and 3-carboxyphenylboronic acid as described in example 88 step 3 (150 mg, yield 16%) as a yellow solid. 1H NMR (300 MHz, DMSO-d6) δ 13.26 (br s, 1H), 8.85 (s, 1H), 8.19 (s, 1H), 8.07-8.05 (m, 2H), 7.96-7.93 (d, J=7.9 Hz, 1H), 7.62-7.57 (t, J=7.7 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-c9ad1765823047ca8c59e2d5bd074706
Source noteuspto-grants-2014_12