HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989346Generated: October 29, 2026
Ammonium Hydroxide → 4-(2,4-Dichloroanilino)-7-hydroxybenzo[g]quinoline-3-carbonitrile
https://huagongshe.com/reaction/989346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | 4-(2,4-Dichloroanilino)-7-methoxybenzo[g]quinoline-3-carbonitrile | HCID 21956392 | — |
| Product | 4-(2,4-Dichloroanilino)-7-hydroxybenzo[g]quinoline-3-carbonitrile | HCID 21956480 | — |
Reaction Steps
A reaction mixture of 566.5 mg (1.44 mmol) of 4-(2,4-dichloroanilino)-7-methoxybenzo[g]quinoline-3-carbonitrile and 10 g of pyridine hydrochloride is stirred at 215° C. for 50 min under nitrogen. After cooling, the mixture is neutralized with 40 mL of a 3% ammonium hydroxide solution and stirred for 0.5 hour. The separated solid is filtered off and washed with water and ether. After drying in vacuo, this yields 527.9 mg (96.5%) of 4-(2,4-dichloroanilino)-7-hydroxybenzo[g]quinoline-3-carbonitrile as a salmon color solid, mp>300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06638929B2 |
|---|
| Source dataset | uspto-grants-2003_10 |
|---|
| ORD ID | ord-90151e72988648c6ae3457cf8af9d2ee |
|---|
| Source note | uspto-grants-2003_10 |
|---|