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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592319Generated: October 31, 2026

Dimethylformamide → HCID 66690761, compound

https://huagongshe.com/reaction/592319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylamineHCID 7912—
Reactant4-Fluorophenylboronic acidHCID 285645—
ReactantMethyl 4-amino-3-bromo-5-nitrobenzoateHCID 13685347—
Catalystpalladium(II) acetateHCID 167845—
CatalystTrisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 66690761HCID 6669076188%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 4-amino-3-bromo-5-nitrobenzoate (1.0 g, 3.64 mmol), (4-fluorophenyl)-boronic acid (0.76 g, 5.45 mmol), 3,3′,3″-phosphinidynetris (benzensulfonic acid) trisodium salt (0.18 g, 0.27 mmol), palladium(II) acetate (20.0 mg, 0.09 mmol) and diisopropylamine (0.52 mL, 3.64 mmol) were added N,N-dimethylformamide (13.6 mL) and water (4.5 mL). The mixture was heated to 80° C. After 1 h, the mixture was cooled to ambient temperature and ethyl acetate was added. The organic layer was dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes→50% hexanes/ethyl acetate) gave the title compound (0.93 g): LC-MS [M+1]=291.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238647B2
Source datasetuspto-grants-2016_01
ORD IDord-507ec2e287054d22a392ae0df278dd3c
Source noteuspto-grants-2016_01