HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576941Generated: October 30, 2026
Benzene → 3-[N-(alpha-chloroacetyl)-2-methyl-4-chloroanilino]propionaldehyde
https://huagongshe.com/reaction/1576941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-(2-Methyl-4-chloroanilino)propionaldehyde | HCID 21510284 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[N-(alpha-chloroacetyl)-2-methyl-4-chloroanilino]propionaldehyde | HCID 21510302 | — |
Reaction Steps
The diethyl acetal of 3-(2-methyl-4-chloroanilino)propionaldehyde (0.2 mole), benzene (150 ml) and sodium carbonate (0.2 mole) dissolved in water (50 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and addition funnel. The mixture is cooled in an ice bath and chloroacetyl chloride (0.2 mole) is added dropwise with stirring. After addition is completed stirring is continued and the reaction mixture is allowed to warm up to room temperature. After this time the mixture is filtered and the filtrate washed with dilute aqueous hydrochloric acid. The washed filtrate is dried over anhydrous magnesium sulphate and is stripped of solvent under reduced pressure to yield the desired product the diethyl acetal of 3-[N-(α-chloroacetyl)-2-methyl-4-chloroanilino]propionaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03983174 |
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| Source dataset | uspto-grants-1976_09 |
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| ORD ID | ord-cce2c93df68940aaa0229d13e320629c |
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| Source note | uspto-grants-1976_09 |
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