Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | 2-(Ethylamino)ethanol | HCID 8072 | — |
| Reactant | Chlorotriethylsilane | HCID 13819 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58815901 | HCID 58815901 | 105.2% |
Reaction Steps
Imidazole (18.15 g) was added to the solution of 2-(ethylamino)ethanol (9.14 g) in CH2Cl2 (200 mL) at room temperature. The mixture was stirred for 10 minutes until all imidazole were dissolved. The solution was cooled in ice bath for 20 minutes. Chlorotriethylsilane (15.46 g) was added to the solution via a syringe. The solution was stirred under nitrogen for overnight, while it was warmed up to room temperature. The reaction solution was washed by H2O (150 mL×3), brine (150 mL×1), dried by Na2SO4 and concentrated to give crude ethyl-(2-triethylsilanyloxy-ethyl)-amine (21.94 g), which was used in next step without further purification. 1H NMR (300 MHz, DMSO-d6) □ 3.58 (t, 2H, J=6.0 Hz), 2.53 (m, 4H), 1.41 (s, 1H), 0.93 (m, 12H), 0.54 (q, 6H, J=8.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07683168B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-dbf33ae88a434cca82f8cbeec6037645 |
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| Source note | uspto-grants-2010_03 |
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