HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HC Yellow no. 14
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Benzonitrile, 4-chloro-3-nitro- | HCID 13655 | — |
| Solvent | Water | HCID 962 | — |
| Product | HC Yellow no. 14 | HCID 15001944 | 96.2% |
Reaction Steps
Monoethanolamine (38 ml; 0.62 mol) was added to a suspension of 4-chloro-3-nitrobenzonitrile (51.6 g; 0.28 mol) in 270 ml water. The reaction mixture was refluxed for one hour at 100°-110° C. (oil bath). After cooling to room temperature, the orange precipitate was filtered, washed with water and air-dried to give 55.8 g 4-(2-hydroxyethylamino)-3-nitrobenzonitrile (m.p.=132°-134° C.). The yield was about 95%, with the overall yield for the reaction sequence, illustrated below, being about 81%. ##STR6##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04980158 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-8f822e722a3a4fa9ae12fe3f33c8666b |
| Source note | uspto-grants-1990_12 |