HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063741Generated: October 31, 2026
Hydrochloric Acid → 1-Dimethylamino-4-[1-(1-ethoxy-ethoxy)-2-phenoxyethyl]cyclohexanecarbonitrile
https://huagongshe.com/reaction/2063741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4-[1-(1-Ethoxy-ethoxy)-2-phenoxyethyl]cyclohexanone | HCID 66886839 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Dimethylamino-4-[1-(1-ethoxy-ethoxy)-2-phenoxyethyl]cyclohexanecarbonitrile | HCID 66886517 | — |
Reaction Steps
40% aqueous dimethylamine solution (1.73 ml, 13.7 mmol) was added to a mixture of 4 M hydrochloric acid (747 μl) and methanol (448 μl), while cooling with ice, and the mixture was added to 4-[1-(1-ethoxy-ethoxy)-2-phenoxyethyl]cyclohexanone (880 mg, 2.87 mmol), before potassium cyanide (448 mg, 6.88 mg) was added. Tetrahydrofuran (3 ml) was also added for solubilization. The reaction mixture was stirred at room temperature for 6 h, water (50 ml) was then added and the mixture was extracted with diethyl ether (4×30 ml). The combined organic phases were concentrated in vacuo, the residue was taken up in methylene chloride (30 ml) and the mixture was washed with water (30 ml). The organic phase was dried with sodium sulfate and concentrated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288406B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-d86665b5a3eb4b22a0700b53a536f38f |
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| Source note | uspto-grants-2012_10 |
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