HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132768Generated: October 31, 2026
1-Bromo-2-methylpropane → HCID 12489470, compound
https://huagongshe.com/reaction/132768
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-oxocyclopentanecarboxylate | HCID 69136 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12489470 | HCID 12489470 | 90% |
Reaction Steps
Under vigorously agitation, 13.9 g of ethyl 2-oxocyclopentane carboxylate was added to 33.4 g of fine powdery anhydrous potassium carbonate and 1.14 g of benzyl triethyl ammonium chloride. After stirring for several minutes, to the mixture was added 60 ml of N,N-dimethyl formamide and 21.9 g of iso-butyl bromide. Upon the completion of the addition, the reaction was heated to 55° C. and allowed to continue for 6 hours with stirring. The solvent was removed under reduced pressure, and solid residue was washed with diethyl ether. The washing liquor was collected and washed with water, and removing the solvent gave a crude product. The crude product was distilled under reduced pressure, and 15.3 g of colorless liquid as a distillate cut of 139-142° C./15 mmHg was colleted. Yield: 90.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07388103B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-be753d3db2e04c4088ca05894f62a8d3 |
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| Source note | uspto-grants-2008_06 |
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