HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dichloroaniline → HCID 68540128, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dichloroaniline | HCID 12281 | — |
| Reactant | HCID 54134744 | HCID 54134744 | — |
| Reactant | HCID 86734205 | HCID 86734205 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68540128 | HCID 68540128 | — |
Reaction Steps
19.2 g of tricyclo-[3.2.2.02.4 ]-nonane-6,7-dicarboxylic acid anhydride (prepared from the cycloheptatriene/maleic acid anhydride adduct (see Ex. 1a) by catalytic hydrogenation, K. Alder, Ber. 86, 1528-39 (1953) and 19.4 g of 3,5-dichloroaniline are refluxed in 1000 ml of toluene for 16 hours, whereby thewater forming during the reaction is separated with a water separator. After cooling, the toluene is removed in vacuum, and the residue recrystallised from ethyl acetate, M.P. 145° - 153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03993662 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-2d77e6d178894028b56d89afd524e95f |
| Source note | uspto-grants-1976_11 |