HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484317Generated: October 31, 2026
Ethyl bromoacetate → HCID 54519729, compound
https://huagongshe.com/reaction/484317
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 19747228 | HCID 19747228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54519729 | HCID 54519729 | 97.2% |
Reaction Steps
Dry THF (20 ml) was added to 0.4 g of 8-cyano-11-(4-piperidylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine to dissolve the latter, followed by the addition of 0.2 g of triethylamine and 0.27 g of ethyl bromoacetate. The resultant mixture was stirred at room temperature for 24 hours. After the completion of the reaction, THF was distilled off under reduced pressure, the residue was dissolved in chloroform, and the resultant solution was washed with water. The chloroform layer was dried over anhydrous Na2SO4 and then filtered. The chloroform was distilled off under reduced pressure. The residue was purified by chromatography on a silica gel column and, from relevant fractions eluted with chloroform:methanol (20:1), 0.5 g of 8-cyano-11-(1-ethoxycarbonylmethyl-4-piperidylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine was obtained (yield: 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05231101 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-5459fe61ea8540e8b176ecb30a487379 |
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| Source note | uspto-grants-1993_07 |
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