HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105472Generated: November 1, 2026
1,1-Dichloroethane → HCID 67506105, compound
https://huagongshe.com/reaction/2105472
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | 4-chloroquinolin-3-amine | HCID 817332 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67506105 | HCID 67506105 | — |
Reaction Steps
A mixture of 3-amino-4-chloroquinoline (8.00 g, 1 eq), trimethylacetyl chloride (11 mL g, 2 eq), and anhydrous dichloroethane (150 mL) was heated at 70° C. After 6 hours more trimethylacetyl chloride (2 eq) was added and heating was continued for a total of 23 hours. The reaction mixture was diluted with dichloromethane, washed sequentially with saturated aqueous potassium carbonate, water, and brine, dried over sodium sulfate, filtered, and then concentrated under reduced pressure. The residue was triturated with hexanes and then filtered to provide 7.16 g of N-(4-chloroquinolin-3-yl)trimethylacetamide as a solid. The filtrate was concentrated under reduced pressure to provide 5 g of crude N-(4-chloroquinolin-3-yl)trimethylacetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07579359B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-fd32fdf9a6d54bb79088cf444f83c055 |
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| Source note | uspto-grants-2009_08 |
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