HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380100Generated: October 30, 2026
Ethyl bromoacetate → HCID 13590327, compound
https://huagongshe.com/reaction/1380100
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | HCID 13590326 | HCID 13590326 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13590327 | HCID 13590327 | 15.7% |
Reaction Steps
A mixture of 5-amino-6,7-dichloro-2-cyclopentyl-2,3-dihydro-2-methyl-1H-inden-1-one (800 mg), postassium carbonate (440 mg), and ethyl bromoacetate (540 mg) in acetone (20 ml) is heated at reflux overnight. The reaction mixture is filtered, the acetone is distilled at reduced pressure and the residual oil is dissolved in a mixture of ethanol (5 ml) and methylene chloride (5 ml) and treated with 10 N sodium hydroxide (2 ml). The mixture is stirred overnight, the solvents are distilled at reduced pressure and the residue is treated with water, then filtered and acidified with hydrochloric acid and extracted with ethyl acetate. Evaporation of the ethyl acetate gives 150 mg of [(6,7-dichloro-2-cyclo-pentyl-2,3-dihydro-2-methyl-1-oxo-1H-inden-5-yl)amino]acetic acid which melts at 199°-200° C. after recrystallization from chloroform-hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04579869 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-f7c128b9cf1e4c2cba6dc35946ed86fe |
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| Source note | uspto-grants-1986_04 |
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