HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957545Generated: November 2, 2026
Chloroacetyl chloride → HCID 19067936, compound
https://huagongshe.com/reaction/1957545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 19067902 | HCID 19067902 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19067936 | HCID 19067936 | 53% |
Reaction Steps
1.68 Grams of 1-(3-aminopropyl)-5,7-diallyl-3,4-dihydro-6-hydroxy-2(1H)-quinolinone was suspended in 100 ml of chloroform, then 5 ml of triethylamine was added thereto and stirred for 30 minutes. Under ice-cooling condition, 2 ml of chloroacetyl chloride was added little by little and stirred for 5 hours. The reaction mixture was washed with water, an aqueous solution saturated with sodium hydrogen carbonate and an aqueous solution saturated with sodium chloride, and dried with anhydrous magnesium sulfate, then concentrated under reduced pressure, there was obtained 1 g (53%) of 1-(3-chloroacetylaminopropyl)-5,7-diallyl-3,4-dihydro-6-hydroxy-2(1H)-quinolinone. White powdery crystals (recrystallized from ethyl acetate-n-hexane). Melting point: 152°-154° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05786367 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-2dc6e8a032b9470bb4510bd285767717 |
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| Source note | uspto-grants-1998_07 |
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