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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912574Generated: October 31, 2026

(3-Chlorophenyl)boronic acid → HCID 59807916, compound

https://huagongshe.com/reaction/912574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
ReactantHCID 59807653HCID 59807653—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventSodium CarbonateHCID 10340—
SolventDimethoxyethane ethanolHCID 20074477—
ProductHCID 59807916HCID 5980791648.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirring solution of 1-(2-bromophenyl)-2,5-dimethyl-1H-pyrrole-3-carboxylic acid (4-methanesulfonyl-phenyl)-amide (100 mg, 0.23 mmol) and 3-chlorophenylboronic acid (0.95 g, 0.57 mmol) in DME/EtOH (2:1, 5 mL), 1M Na2CO3 (0.80 mL) and Pd(dppf)2Cl2 (38 mg, 0.046 mmol) were added. The reaction mixture was degassed and heated at 80° C. under Argon for 1 h and monitored by LC-MS. The mixture was diluted with DCM (20 mL) and washed with 15 mL of brine. The aqueous phase was extracted with DCM (20 mL) twice. The combined extracts were dried over anhyd Na2SO4 and concentrated under reduced pressure. The crude residue was purified by flash chromatography on silica gel, eluting with EtOAc-Hex (0-50%) to yield the title compound (53 mg, 48%) as a pale yellow solid. 1H-NMR (CDCl3): δ 7.89 (2H, d), 7.80 (2H, d), 7.65 (1H, s), 7.57 (3H, m), 7.26 (3H, m), 7.04 (1H, t), 6.87 (1H, m), 6.13 (1H, s), 3.03 (3H, s), 2.23 (3H, s), 1.89 (3H, s). MS (ESI): 479 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026237B2
Source datasetuspto-grants-2011_09
ORD IDord-d03421bf465741ca87c92357e68b9c68
Source noteuspto-grants-2011_09