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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629771Generated: November 1, 2026

N-Methyl dicyclohexylamine → HCID 86685861, compound

https://huagongshe.com/reaction/1629771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl dicyclohexylamineHCID 24210—
ReactantEthyl trans-crotonateHCID 429065—
ReactantHCID 21931268HCID 21931268—
CatalystTetraethylammonium ChlorideHCID 5946—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylacetamideHCID 31374—
ProductHCID 86685861HCID 8668586157.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

Intermediate 11A (2.81 g, 9.93 mmol), (E)-ethyl but-2-enoate (1.25 g, 10.9 mmol), palladium(II) acetate (0.11 g, 0.5 mmol), tetraethylammonium chloride (1.65 g, 9.9 mmol), N-cyclohexyl-N-methylcyclohexanamine (2.91 g, 14.9 mmol) and dimethylacetamide (30 ml) were placed in a oven-dried vial and sparged with argon for 5 min. The vial was sealed and the reaction heated to 110° C. for 6 h. The reaction was cooled to rt, diluted with EtOAc (75 mL), washed with water and sat'd aq NaCl, dried over anhydrous MgSO4, filtered and concentrated. The residue was purified by silica gel chromatography eluting with EtOAc in hexanes to provide Intermediate 11B (1.81 g, 49%) as a colorless oil. LCMS Anal. Calc'd for C16H19F3O3 316.32, found [M+H] 317.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791091B2
Source datasetuspto-grants-2014_07
ORD IDord-590696793d6946d0802d8f78f838db30
Source noteuspto-grants-2014_07