HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921840Generated: October 30, 2026
N-Methyl dicyclohexylamine → HCID 89922748, compound
https://huagongshe.com/reaction/921840
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methyl dicyclohexylamine | HCID 24210 | — |
| Reactant | 3-Buten-1-ol | HCID 69389 | — |
| Reactant | 2-(Di-tert-butylphosphino)-2'-methyl-1,1'-biphenyl | HCID 2734937 | — |
| Reactant | 5-Amino-2-bromo-4-chlorobenzonitrile | HCID 53216229 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 89922748 | HCID 89922748 | 23.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273057B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-0f4bb32eddc3463780d0ae6a7a871ff0 |
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| Source note | uspto-grants-2016_03 |
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