HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-(2-Cyanoethylidene)-bicyclo[2.2.1]heptane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Bicyclo[2.2.1]heptane-2-carbaldehyde | HCID 86864 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(2-Cyanoethylidene)-bicyclo[2.2.1]heptane | HCID 54423975 | 79% |
Reaction Steps
A stirred solution of 95 g (0.77 mol) of 2-formylbicyclo[2.2.1]heptane, 65 g (0.76 mol) of cyanoacetic acid, 2 ml of ammonium hydroxide (58%), 132 ml of dimethylformamide, and 170 ml benzene was heated to reflux and the water removed with a Dean-Stark trap. The reaction was allowed to continue until the evaluation of carbon dioxide ceased (approx. 24 hrs.). Upon completion, the reaction was cooled and the solvent removed under reduced pressure. The residual oil was distilled under vacuum to give 88 g (79% yield) of 2-(2-cyanoethylidene)-bicyclo[2.2.1]heptane: b.p. 72-80° C/1 mm; ir 2960, 2870, 2260, 1685, 1450, 1420, 1305, 920; nmr 1.15-2.8 (10H, m), 2.96 (2H, m) 4.9-5.4 (1H, m); ms 147.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04132677 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-3bf553e8b90e4140a4669feace17b8f4 |
| Source note | uspto-grants-1979_01 |