HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrobenzaldehyde → HCID 20306576, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | 3,4-Dihydro-2H-1-benzopyran-4-amine | HCID 4961957 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20306576 | HCID 20306576 | — |
Reaction Steps
An 80 g, (0.54 mole) portion of 4-chromanamine, and 650 ml of ethanol were placed in a 2-l, 3-necked flask, equipped with a stirrer and reflux condenser fitted with a drying tube. The slurry was treated with 85 g (0.56 mole) portion of m-nitrobenzaldehyde using rapid mechanical stirring. The reaction mixture was refluxed for 5 hrs., cooled 1 hr. and filtered. The yellow crystalline solid was washed with 100 ml of ethanol, ether, and dried, m.p. 117°-118°. Yield: 115 g (76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04115407 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-af9017eba49b4999841395986d2365b4 |
| Source note | uspto-grants-1978_09 |