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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019325Generated: November 1, 2026

Oxygen → HCID 12467353, compound

https://huagongshe.com/reaction/1019325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantSodium CyanideHCID 8929—
ReactantN-Ethyl-N-methylanilineHCID 11956—
ReactantSodium BicarbonateHCID 516892—
ReactantAcetic acid methanolHCID 10129899—
ProductHCID 12467353HCID 12467353—

Reaction Conditions

Temperature60 °C

Reaction Steps

N-ethyl-N-methylaniline (1 mmol), RuCl3-nH2O (0.05 mmol) and sodium cyanide (1.2 mmol) were charged into a 25-ml side-arm flask, the interior of the reacting container was replaced by oxygen, and an oxygen balloon was attached to supply oxygen at 1 atm. Then, 1.7 ml of a mixed solvent of methanol-acetic acid (volume ratio 3/1) was added thereto at room temperature. Reaction was effected by stirring the mixed liquid at 60° C. for 24 hours. After the reaction mixture liquid was made alkaline with the addition of saturated sodium bicarbonate aqueous solution, the mixture was extracted with 10 ml ethyl acetate once and with 5 ml ethyl acetate twice. The extracted liquid thus obtained was washed with saturated saline solution, and dried over sodium sulfate, thereby obtaining an ethyl acetate solution of N-phenyl-N-ethylaminoacetonitrile and 2-(N-methyl-N-phenylamino)propionitrile. This solution was analyzed by a gas chromatography internal standard method, which revealed the conversion rate of N-ethyl-N-methylaniline being 70% with a yield of N-phenyl-N-ethylaminoacetonitrile being 57% (vs. N-ethyl-N-methylaniline) and that of 2-(N-methyl-N-phenylamino)propionitrile being 7% (vs. N-ethyl-N-methylaniline).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486340B2
Source datasetuspto-grants-2002_11
ORD IDord-0c48018a8b5040f1ac1989a6922b3099
Source noteuspto-grants-2002_11