HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371708Generated: October 27, 2026
Dimethylformamide → Ethyl 4-(dibenz[b,e]oxepin-11(6H)-ylidene)-1-piperidinepropionate
https://huagongshe.com/reaction/2371708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3-bromopropionate | HCID 68320 | — |
| Reactant | 4-(dibenz[b,e]oxepin-11(6H)-ylidene)piperidine | HCID 9947379 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-(dibenz[b,e]oxepin-11(6H)-ylidene)-1-piperidinepropionate | HCID 10276748 | 85.5% |
Reaction Steps
A mixture of 3.61 g of 4-(dibenz[b,e]oxepin-11(6H)-ylidene)piperidine, 2.6 g of ethyl 3-bromopropionate, 1.8 g of potassium carbonate and 25 ml of N,N-dimethylformamide was stirred at 80° C. for 2 hrs. After cooling, water was added to the reaction mixture and extracted with ether. The ether layer was washed with water and extracted with hydrochloric acid. The aqueous layer was made alkaline with potassium carbonate and extracted with ether. The ether layer was washed with water, dried and concentrated to give 4.2 g of yellowish brown liquid, which was purified by column chromatography on silica gel (eluent: chloroform) to give 3.9 g of pale yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05095022 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-1ecece786d914257a0bd871fa5431f8c |
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| Source note | uspto-grants-1992_03 |
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