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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097209Generated: October 25, 2026

Dimethylformamide → 2-Chlorocyclohex-1-ene-1-carbonitrile

https://huagongshe.com/reaction/1097209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCyclohexanoneHCID 7967—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventWaterHCID 962—
Product2-Chlorocyclohex-1-ene-1-carbonitrileHCID 4984093939%

Reaction Steps

To an ice cold (0-5° C.) solution of dry dimethylformamide (6.67 mL, 86.5 mmol) was added phosphorous oxychloride (7.66 mL, 81.6 mmol) dropwise with stirring for 15 min. To this cold mixture, cyclohexanone (5 g, 51 mmol) was added dropwise maintaining the temperature of the reaction mixture below 40° C. for 1 h. Hydroxylamine hydrochloride (20 g, 288 mmol) was added portion wise for 20 min. The addition of hydroxylamine hydrochloride was maintained at such a rate that the temperature of the reaction mixture rise above 145-155° C. After completion of the addition, the reaction mixture was allowed to room temperature (rt) for 30 min, diluted with cold water (0.5 L) and stirred for 30 min. The precipitated solid was filtered, washed with cold water and dried to give the product as a brown color solid (2.8 g, 39%), mp 38-40° C. 1H NMR (400 MHz, CDCl3): δ 2.45-2.50 (2H, m, H-6), 2.33-2.37 (2H, m, H-3), 1.75-1.81 (2H, m, H-5), 1.66-1.72 (2H, m, H-4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143237B2
Source datasetuspto-grants-2012_03
ORD IDord-a3969f3f7139455196c057472a855b0c
Source noteuspto-grants-2012_03