HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Tert-butyl 2-(benzyl(methyl)amino)ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | N-Benzyl-N'-boc-ethylenediamine | HCID 10634443 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Tert-butyl 2-(benzyl(methyl)amino)ethylcarbamate | HCID 50999034 | 46.8% |
Reaction Steps
To a mixture of tert-butyl 2-(benzylamino)ethylcarbamate (2.8 g, 11.2 mmol) and 37% aqueous CH2O (1.0 mL, 11.2 mmol) in 1,2-dicholoroethane (35 mL) at RT was added NaHB(AcO)3 (3.7 g, 11.2 mmol). The mixture was stirred (RT, 16 h), diluted with saturated aqueous NaHCO3 (400 mL) and extracted with EtOAc (3×300 mL). The organic layer was dried over MgSO4 and concentrated under reduced pressure to afford tert-butyl 2-(benzyl(methyl)amino)ethylcarbamate (1.38 g, 46.8%). 1HNMR (CDCl3): δ 7.25 (m, 5H, CH), 3.5 (s, 2H, CH2), 3.3 (m, 2H, CH2), 2.48 (m, 2H, CH2), 2.2 (s, 3H, CH3), 1.4 (s, 9H, CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846972B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-cfde26ee55314891aa66161472e44241 |
| Source note | uspto-grants-2014_09 |