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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271891Generated: November 1, 2026

Dimethylacetamide → HCID 58847064, compound

https://huagongshe.com/reaction/1271891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
ReactantHCID 18455603HCID 18455603—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystZincHCID 23994—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystHCID 145821890HCID 145821890—
ProductHCID 58847064HCID 58847064—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 5-bromo-2-(2,6-dimethylmorpholin-4-yl)benzaldehyde (0.298 g, 1.00 mmol), 1,1′-bis(dimethylphosphino)ferrocene [dppf] (0.022 g, 0.040 mmol), tris(dibenzylideneacetone)dipalladium [Pd2(dba)3] (0.018 g, 0.020 mmol), zinc dust (0.008 g, 0.12 mmol) and zinc cyanide (0.070 g, 0.60 mmol) in dimethylacetamide (2 mL) is heated 120° C. for 4 h. The reaction mixture is cooled and partitioned between dilute ammonium hydroxide and ethyl acetate. The phases are separated. The organic layer is extracted with an additional portion of ethyl acetate. The combined organic layers are dried (NaSO4) and then concentrated. The resulting residue is purified by silica gel chromatography using ethyl acetate-methylene chloride-heptane (0.5:4.0:5.5) as the eluent to afford, 172 mg (70%) of the cyano aldehyde. 1H NMR (400 MHz, CDCl3) δ 10.05, 7.97, 7.64, 7.01, 3.92–3.79, 3.14, 2.70, 1.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208490B2
Source datasetuspto-grants-2007_04
ORD IDord-0def5038b85b42fd87ba454c808f88cc
Source noteuspto-grants-2007_04