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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335216Generated: October 25, 2026

Diisopropylamine → Methyl 4-bromo-2-methoxy-2-methylpent-4-enoate

https://huagongshe.com/reaction/335216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant2,3-DibromopropeneHCID 10552—
ReactantPropanoic acid, 2-methoxy-, methyl esterHCID 86599—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-bromo-2-methoxy-2-methylpent-4-enoateHCID 86631519109.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 500 mL round-bottom flask was charged with diisopropylamine (12.89 mL, 92.00 mmol) and dry THF (100 mL) and cooled to −78° C. Butyllithium (2.5 M in hexanes) (36.80 mL, 92.00 mmol) was added dropwise over 20 minutes and the mixture was agitated for additional 30 minutes. Methyl 2-methoxypropanoate (10.35 g, 87.61 mmol) was added dropwise over 20 minutes and the mixture was agitated for 30 minutes. 2,3-Dibromopropene (10.70 mL, 87.61 mmol) was added dropwise over 20 minutes, the mixture was agitated for 30 minutes and then allowed to warm up to ambient temperature and agitated for additional 2 hours. The reaction was quenched with saturated ammonium chloride solution and extracted twice with ether. Extracts were washed with sodium bicarbonate solution, brine, dried and evaporated to give the title compound (22.7 g, 98.4% yield) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883828B2
Source datasetuspto-grants-2014_11
ORD IDord-12a6afb9c809476f8edb0aaaa2d93ddc
Source noteuspto-grants-2014_11