HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 2-(4-Carboethoxy-1-piperidylmethyl)propenenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(4-Carboethoxy-1-piperidylmethyl)propenenitrile | HCID 13037609 | — |
Reaction Steps
Cyanoacetic acid (8.6 g., 0.1 mole) was dissolved in 35 ml. of dioxane. 4-Carboethoxypiperidine (15.7 g., 0.1 mole) was added--a precipitate rapidly formed. When one-half was added 10 ml. of water was then admixed and the temperature controlled below 24° C. until complete addition. With ice bath cooling, 37% aqueous formaldehyde (18 g., 0.2 mole) was dripped in over an 8-minute period and the temperature allowed to rise to 29° C. accompanied by vigorous carbon dioxide evolution. Two phases separated and stirring was continued for an additional 12 hours. After concentration in a bath at 45° C. and under reduced pressure, 22.4 g. of an oil resulted. The product was distilled, b.p., 130°-132° C./0.6 mm., yield, 16.3 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04391812 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-531e7c4bc2614d47a2f26a0c41416037 |
| Source note | uspto-grants-1983_07 |