HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 9-Benzoyl-8-bromo-1,2,3,4-tetrahydrocarbazole-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Oxocyclohexanecarboxylic acid | HCID 192730 | — |
| Reactant | Acetaldehyde 1-benzoyl-1-(2-bromophenyl)hydrazone | HCID 68139504 | — |
| Reactant | Acetaldehyde 2-bromophenyl hydrazone | HCID 86733215 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 9-Benzoyl-8-bromo-1,2,3,4-tetrahydrocarbazole-3-carboxylic acid | HCID 21548627 | — |
Reaction Steps
A solution of acetaldehyde 1-benzoyl-1-(2-bromophenyl)hydrazone, prepared from 11 g. of acetaldehyde 2-bromophenyl hydrazone (see below), and 9.16 g. of cyclohexanone-4-carboxylic acid in 25 ml. glacial acetic acid was heated on a hot plate until evolution of acetaldehyde was no longer detected (about two hours), 25 ml. glacial acetic acid saturated with hydrogen chloride was added and heating was continued for 30 minutes. The mixture was cooled and cautiously diluted with water, and the resulting solid was collected by filtration and washed with water to give 2.24 g. of the title compound; m.p. 196°-198°C. (chloroform-heptane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03948939 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-f6ccce52625749f6b08db8e5fc5078c1 |
| Source note | uspto-grants-1976_04 |