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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396787Generated: October 30, 2026

2-Butene, 1-bromo-3-methyl- → HCID 18922258, compound

https://huagongshe.com/reaction/2396787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butene, 1-bromo-3-methyl-HCID 70092—
ReactantLithium diisopropylamideHCID 2724682—
ReactantMethyl N-(tert-butoxycarbonyl)-N-methylglycinateHCID 14018930—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18922258HCID 1892225863.7%

Reaction Steps

A 2 M solution of LDA (70.32 ml, 0.14 mol) was added (via syringe) to a solution of N-t-butoxycarbonyl-sarcosine methyl ester (26 g, 0. 1279 tool) in 40 ml of dry THF at -78° C. under nitrogen and the mixture was stirred at this temperature for 30 minutes. To the above mixture was added 4 -bromo-2-methyl-2-butene (20 g, 0.134 mol) with stirring continuing at -78° C., and the resulting mixture was allowed to warm to room temperature. The reaction mixture was quenched with a saturated ammonium chloride solution at -78° C, and then water was added, and the resulting reaction mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over sodium sulfate, and concentrated in vacuo to yield a yellow oil, which was purified by silica gel column chromatography (20% ethyl acetate in hexane) to afford 22.1 g (63.7 %) of N-t-butoxycarbonyl-2-(3-methyl-2-butenyl) sarcosine methyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05494925
Source datasetuspto-grants-1996_02
ORD IDord-0e411d8e6fe54150a26d9635fa417368
Source noteuspto-grants-1996_02