HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxybenzylamine → Tert-butyl (2-methoxybenzyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxybenzylamine | HCID 81292 | — |
| Reactant | Tert-butyldicarbonate | HCID 22064466 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl (2-methoxybenzyl)carbamate | HCID 22926021 | 84.5% |
Reaction Steps
13.0 g of 2-methoxybenzylamine was dissolved in 80 ml of tetrahydrofuran, and tetrahydrofuran solution (20 ml) containing 16 g of t-butyldicarbonate was added, followed by stirring for 1 hour at room temperature. The solvent was evaporated, and the residue was dissolved in ethyl acetate and successively washed with 1 N hydrochloric acid and saturated brine. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was evaporated, to give 19.0 g of t-butyl N-(2-methoxybenzyl)carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244861B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-cc36d635ea604f5eb39d34b499fcf0d6 |
| Source note | uspto-grants-2007_07 |