HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → 5-Cyanogramine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Indole-5-carbonitrile | HCID 27513 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Cyanogramine | HCID 33033 | 100% |
Reaction Steps
To a solution of 14.0 g (98.5 mmol, 1.0 equiv.) of 5-cyanoindole in 35 mL of ethanol was added 8.7 mL (108 mmol, 1.1 equiv.) of 40% aqueous formaldehyde and 12.2 mL (108 mmol, 1.1 equiv) of 40% aqueous dimethylamine. The flask was fitted with a reflux condenser topped with a cold finger condenser at -78° C. The solution was heated to reflux for eight hours at which time TLC indicated absence of starting material. The solution was poured into 350 mL of chloroform and washed once with 50 mL of 10% aqueous sodium carbonate. The organic layer was separated, dried over anhydrous sodium sulfate, filtered and concentrated to yield 19.6 g (100%) of 5-cyano-3-(dimethylamino)methyl-1H-indole, pure by 1H NMR analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05300506 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-6e5e2b06f50946749f1acb867dc988ef |
| Source note | uspto-grants-1994_04 |