HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 12330905, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12330905 | HCID 12330905 | — |
Reaction Steps
A solution of acetophenone (120 ml), o-anisidine (123 ml), benzene (100 ml) was refluxed with continuous removal of water. The crude product was purified by crystallizing it from ethanol to give N-(αmethyl benzylidene)-o-anisidine (IX) (90 C). It was then hydrogenated using 5% Pd/C as the catalyst and 95% ethanol as the solvent to give N-(α-methyl benzyl)-o-anisidine (X). X had a boiling point of 117° C. at 0.3 millimeter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04962234 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-857e6ff67a7242aca650c6eb367ef29a |
| Source note | uspto-grants-1990_10 |