HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589309Generated: October 30, 2026
Chloroacetyl chloride → 1-(Chloroacetyl)-7-nitro-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/589309
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | 7-Nitro-1,2,3,4-tetrahydroquinoline | HCID 252513 | — |
| Reactant | Ethylacetate heptane | HCID 21899848 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(Chloroacetyl)-7-nitro-1,2,3,4-tetrahydroquinoline | HCID 12578360 | — |
Reaction Steps
1.78 g of 7-nitro-1,2,3,4-tetrahydroquinoline (0.01 mol) are dissolved in 15 ml of ethyl acetate. This solution is run into a mixture of 15 ml of ethyl acetate and 0.80 ml of chloroacetyl chloride. A white precipitate forms immediately, and stirring is continued at 30° C. for 2 h (the reaction is monitored by thin layer chromatography (90/10 ethyl acetate/heptane)). After 2 h, since the reaction is incomplete, 0.2 equivalent of chloroacetyl chloride is added and the temperature is raised to 60° C.; the solid formed undergoes dissolution. When the reaction has finished, the medium is cooled and the solvent is evaporated off. 2.46 g of a beige product which corresponds to the expected compound are recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09233060B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-0788a70ffbfe4bacbc600c4d6895a47e |
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| Source note | uspto-grants-2016_01 |
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