HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 22163145, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Ethyl 3-aminobenzoate | HCID 11400 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22163145 | HCID 22163145 | — |
Reaction Steps
A solution of acetophenone (95 ml), m-carbethoxy aniline (75 ml), benzene (150 ml) was refluxed in the presence of molecular sieve (50 g) with continuous removal of water. The crude product was distilled under reduced pressure to give N-(α-methyl benzylidene)-m-carbethoxyaniline (XIII). XIII had a boiling point of 205° C. at 0.1 millimeter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04962234 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-da9e7ada385e4e0a8d04f05d31129eb4 |
| Source note | uspto-grants-1990_10 |