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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529292Generated: November 1, 2026

Magnesium Bromide → HCID 118194622, compound

https://huagongshe.com/reaction/529292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMagnesium BromideHCID 82241—
ReactantTrimethyl[(1,2,2-triethoxyethenyl)oxy]silaneHCID 12614350—
ReactantCyclohexane ethylacetateHCID 21867204—
ReactantHCID 118201132HCID 118201132—
SolventTolueneHCID 1140—
ProductHCID 118194622HCID 11819462257.1%

Reaction Steps

N-(2-cyclobutylethylidene)-1-phenylmethanamine (1.00 g, 5.3 mmol) was dissolved in 23 mL toluene, MgBr2.0Et2 (2.07 g, 8.0 mmol) was added and the mixture was stirred at room temperature for 15 minutes. Trimethyl(1,2,2-triethoxyvinyloxy)silane (1.83 g, 7.4 mmol) was added, and the mixture was stirred at room temperature. After 3 hours, the reaction was quenched with water (30 mL) and acidified to pH=2 with hydrochloric acid. The organic phase was washed with sat. NaHCO3, dried over Na2SO4 and the solvent was removed under vacuum to yield the crude product. Column chromatography (silica, cyclohexane:ethyl acetate 10:1) yielded 1.1 g ethyl 3-(benzylamino)-4-cyclobutyl-2,2-diethoxybutanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346853B2
Source datasetuspto-grants-2016_05
ORD IDord-48ebae4860504e72a7cd92e8ed05a9c3
Source noteuspto-grants-2016_05