HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389383Generated: November 2, 2026
Ethyl bromoacetate → HCID 86637916, compound
https://huagongshe.com/reaction/2389383
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 68535385 | HCID 68535385 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86637916 | HCID 86637916 | — |
Reaction Steps
To a solution of 5-(diphenylmethyl)-1-[(2E)-3-(1H-indol-4-yl)-2-propen-1-yl]-2(1H)-pyridinone (80 mg), K2CO3 (80 mg) and benzyltriethylammonium chloride (8.8 mg) in 2-butanone (1 mL) was added ethyl bromoacetate (96 mg) at ambient temperature. The reaction mixture was stirred for 5 hours at 80° C. The resulting mixture was diluted with EtOAc and washed successively with water and brine. The organic layer was dried over anhydrous MgSO4, filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography (chloroform:MeOH=100:0-97:3) to give ethyl (4-{(1E)-3-[5-(diphenylmethyl)-2-oxo-1(2H)-pyridinyl]-1-propen-1-yl}-1H -indol-1-yl)acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273745B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-a0d595fae97a495ab1e960426963b5d8 |
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| Source note | uspto-grants-2012_09 |
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