HuagongsheHuagongshe Chemistry Print Report · For research reference only
Magnesium Bromide → HCID 118194622, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Magnesium Bromide | HCID 82241 | — |
| Reactant | Trimethyl[(1,2,2-triethoxyethenyl)oxy]silane | HCID 12614350 | — |
| Reactant | Cyclohexane ethylacetate | HCID 21867204 | — |
| Reactant | HCID 118201132 | HCID 118201132 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 118194622 | HCID 118194622 | 57.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346853B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-48ebae4860504e72a7cd92e8ed05a9c3 |
| Source note | uspto-grants-2016_05 |