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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132772Generated: October 31, 2026

1-Bromo-3-methylbutane → HCID 69198393, compound

https://huagongshe.com/reaction/132772

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-methylbutaneHCID 7891—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-oxocyclopentanecarboxylateHCID 69136—
SolventAcetoneHCID 180—
ProductHCID 69198393HCID 6919839372.6%

Reaction Steps

Under vigorous agitation, 34.67 g (purity of 90%) of ethyl 2-oxocyclopentane carboxylate was added to 112.65 g (purity of 98%,) of ground anhydrous potassium carbonate, and after stirring for several minutes, to the mixture was added 100 ml of acetone. The reaction mixture was further stirred for about 15 minutes, then thereto was dropwise added 51.36 ml (purity of 98%) of 1-bromo-iso-pentane. Upon the completion of the addition, the reaction mixture was heated for reflux for 6 hours. The reaction mixture was filtered under the reduced pressure, and the filter cake was washed with diethyl ether until its color was purely white. Pale yellow filtrate was collected and dried over anhydrous magnesium sulfate, then the solvent was removed. The residue was distilled under reduced pressure, and 32.80 g of colorless liquid as a distillate cut of 142-147° C./15 mmHg was collected. Yield: 72.60%. MS: m/e 227(M30 +1), 226(M+), 211 (M+—CH3) 198(M+—CH2CH2) 171 (M+—OCH2CH3), 156 (M+—C5H11, base), 153(M+—CO2 CH2CH3), 127(155-CH2CH2), 111(156-OCH2CH3), 55.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388103B2
Source datasetuspto-grants-2008_06
ORD IDord-29f1dbeff6d843b28fb3e5e02ba1f47d
Source noteuspto-grants-2008_06