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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921840Generated: October 30, 2026

N-Methyl dicyclohexylamine → HCID 89922748, compound

https://huagongshe.com/reaction/921840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl dicyclohexylamineHCID 24210—
Reactant3-Buten-1-olHCID 69389—
Reactant2-(Di-tert-butylphosphino)-2'-methyl-1,1'-biphenylHCID 2734937—
Reactant5-Amino-2-bromo-4-chlorobenzonitrileHCID 53216229—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 89922748HCID 8992274823.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

5-amino-2-bromo-4-chlorobenzonitrile (4 g, 17.28 mmol) and N-cyclohexyl-N-methylcyclohexanamine (5.55 mL, 25.9 mmol) were combined in a 250 ml flask and 2 ml of DMF was added. The flask was evacuated and backfilled with Ar 4×. A suspension of Pd2 (dba)3 (0.316 g, 0.346 mmol) and di-tert-butyl(2′-methyl-[1,1′-biphenyl]-2-yl)phosphine (0.324 g, 1.037 mmol) in CH3CN (32 mL) was heated at 60° C. for 1 min until the solids dissolved and then cooled to room temperature. The solution was added to the flask by syringe, and then but-3-en-1-ol (1.933 mL, 22.46 mmol) was added. The reaction was heated at 90° C. for 45 min. The reaction was cooled to room temperature and diluted with H2O, extracting 3× with EtOAc. The organic layers were dried over Na2SO4, filtered, and concentrated. The material was purified by flash column chromatography (0-70% EtOAc/Hex; 330 g column). 5-amino-4-chloro-2-(4-oxobutyl)benzonitrile (0.9 g) was obtained as yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273057B2
Source datasetuspto-grants-2016_03
ORD IDord-0f4bb32eddc3463780d0ae6a7a871ff0
Source noteuspto-grants-2016_03