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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689466Generated: October 31, 2026

Ethyl isobutyrate → Ethyl 7-bromo-2,2-dimethylheptanoate

https://huagongshe.com/reaction/1689466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isobutyrateHCID 7342—
ReactantDiisopropylamineHCID 7912—
Reactant1,5-DibromopentaneHCID 8100—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 7-bromo-2,2-dimethylheptanoateHCID 11265571—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of diisopropylamine (5.82 mL) in THF (30 mL) was added n-butyllithium (2.5M in hexanes, 16.4 mL) at 0° C. and the mixture was stirred for 30 min at this temperature before being cooled to −78° C. Ethyl isobutyrate (5 mL) was added dropwise and the resultant mixture was stirred at −78° C. for 1 h before addition of 1,5-dibromopentane (5.61 mL). The reaction mixture was stirred at −78° C. for 1 h then at RT for 2.5 h before being poured into saturated ammonium chloride solution. The solution was extracted with ethyl acetate (×2), then the combined organics were washed with water and dried over sodium sulphate, filtered and evaporated in vacuo. Purification was by silica gel chromatography eluting with 0-25% ethyl acetate in cyclohexane to give the subtitled compound as a yellow liquid. Yield 4.45 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-3725100818c848f5b7c673f9262bc886
Source noteuspto-grants-2012_04