HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloroaniline → 1-(4-Chloroanilino)phthalazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | 1(2H)-Phthalazinone | HCID 8394 | — |
| Reactant | 1-Chlorophthalazine | HCID 160793 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 1-(4-Chloroanilino)phthalazine | HCID 22741997 | — |
Reaction Steps
30 g (149 mmol) 1-chlorophthalazine (prepared from phthalazone in the manner described under Example 67A.1) and 20 g (157 mmol) 4-chloroaniline are heated in 630 ml n-butanol for 30 min to 65° C. The crude product is filtered off, washed with ether, taken up in 2 l di-chloromethane/methanol 9:1, and washed with sat. NaHCO3 solution and brine. The aqueous phases are extracted three times with dichloromethane/methanol 9:1, the organic phases dried (Na2SO4), and evaporated to a residual volume of ≈50 ml, leading to crystallization of the title compound: m.p.: 211° C.; Anal. calc.(C14H10N3Cl) C, 65.76%; H, 3.94%; N, 16.43%, Cl, 13.86%. found C, 66.02%; H, 3.92%; N, 16.53%, Cl, 13.51%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06710047B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-533cdc17081f491db89c781699e36145 |
| Source note | uspto-grants-2004_03 |