HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973044Generated: October 31, 2026
3,4-Dichloroaniline → HCID 22763481, compound
https://huagongshe.com/reaction/1973044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichloroaniline | HCID 7257 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzenediazonium, 3,4-dichloro-, chloride | HCID 10262515 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 86733168 | HCID 86733168 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 22763481 | HCID 22763481 | — |
Reaction Steps
Prepare a solution of 3,4-dichlorophenyl-diazonium chloride by treating 8.2 g. of 3,4-dichloroaniline in 25 ml of concentrated hydrochloric acid with a solution of 3.5 g. of sodium nitrite in 35 ml of water at -5°. Dissolve ethyl 2-(2,4-dichlorobenzyl) acetoacetate (14.3 g.) in 100 ml of ethanol with 8.3 g. of potassium hydroxide in 8.3 ml of water and cool to -5°. Add the solution of the diazonium salt to the latter solution, keeping the temperature at 0°, and stir for 15 minutes. Extract with ether and wash the ether solution with two 75 ml portions of 5% sodium hydroxide and then with water and dry (MgSo4). Evaporate to yield the intermediate: ethyl 2,4-dichlorophenylpyruvate 3,4-dichlorophenyl hydrazone. The analytical sample is obtained from ethanol; m.p. 160°-161°. Dissolve the hydrazone (125 g.) in 700 ml of 20% ethanolic sulfuric acid and boil under reflux for 2 hours. Cool to room temperature and collect the crystalline product. Wash with 50% aqueous alcohol. Recrystallize from ethanol; m.p. 230°-231°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03996159 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-3aa0f7c9cca744088f10f0926847cfc8 |
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| Source note | uspto-grants-1976_12 |
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