HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Dimethylamino-(1,4-dioxaspiro[4.5]dec-8-yl)-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1,4-Dioxaspiro(4.5)decane-8-carbaldehyde | HCID 9898947 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Dimethylamino-(1,4-dioxaspiro[4.5]dec-8-yl)-acetonitrile | HCID 57839521 | — |
Reaction Steps
40% aqueous dimethylamine solution (85 ml, 0.67 mole), 1,4-dioxa-spiro-[4.5]decane-8-carbaldehyde 5 (240 g, 0.141 mole) and potassium cyanide (22.05 g, 0.338 mole) were added while cooling with ice to a mixture of 4N hydrochloric acid (37 ml) and methanol (22 ml). The mixture was stirred for four days at room temperature and then, after adding water (80 ml), extracted with diethyl ether (4×100 ml). The organic phase was dried over sodium sulfate, concentrated by evaporation in vacuo, and the product was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728028B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-85f0a1c8da154ceeb53790dd29fb205d |
| Source note | uspto-grants-2010_06 |