HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35679Generated: October 29, 2026
Ethyl formate → 6-Chloro-3-hydroxymethylene-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/35679
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | 6-Chloro-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline | HCID 14501422 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Chloro-3-hydroxymethylene-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline | HCID 67872180 | 75.1% |
Reaction Steps
A mixture of 6-chloro-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline(200.5 g) and 1,5-diazabicyclo[5,4, 0] undecene-5(384.9 g) in ethyl formate(400.9 g) was heated at 55° C. with stirring for 7 hours and then diluted with cold water(450 ml). The mixture was washed successively with diisopropyl ether and ethyl acetate and then the aqueous layer was acidified with hydrochloric acid under ice cooling. The resultant precipitate was collected by filtration and dried to give 6-chloro-3-hydroxymethylene-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline(168.29 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04767780 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-6cf4e8aa67054fda944c45da66d14c6b |
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| Source note | uspto-grants-1988_08 |
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