HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malononitrile → HCID 10448627, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-Fluorobenzaldehyde | HCID 68009 | — |
| Reactant | 4-Hydroxy-1-methylindole | HCID 15825739 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10448627 | HCID 10448627 | 30.5% |
Reaction Steps
To a mixture of 3-fluorobenzaldehyde (46 mg, 0.37 mmol) and malononitrile (25 mg, 0.37 mmol) in ethanol (1 mL) was added 4-hydroxy-1-methyl-indole (55 mg, 0.37 mmol) followed by piperidine (0.02 mL, 0.19 mmol, 0.5 eq.). Reaction mixture was stirred at room temperature overnight. The desired compound precipitated and was collected, washed with ethanol and dried, yielding 36 mg of a yellow solid. 1H NMR (CDCl3): 7.28-7.23 (m, 1H), 7.05-7.01 (m, 3H), 6.92-6.86 (m, 2H), 6.74 (d, J=8.4 Hz, 1H), 6.56 (d, J=3.1 Hz, 1H), 4.84 (s, 1H), 4.67 (s, 2H), 3.76 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07528164B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-2ef0a8c177d74bf8868558a0c221f92c |
| Source note | uspto-grants-2009_05 |