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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chlorocyclohex-1-ene-1-carbonitrile | HCID 49840939 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143237B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-a3969f3f7139455196c057472a855b0c |
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| Source note | uspto-grants-2012_03 |
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