HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzylamine hydrochloride → 2-Bromo-N-(tert-butoxycarbonyl)benzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzylamine hydrochloride | HCID 2724202 | — |
| Reactant | Tert-butyldicarbonate | HCID 22064466 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-N-(tert-butoxycarbonyl)benzylamine | HCID 7018300 | 82.9% |
Reaction Steps
15.0 g of 2-Bromobenzylamine hydrochloride was dissolved in 100 ml of tetrahydrofuran, and a solution of 13 g of t-butyl dicarbonate in tetrahydrofuran (25 ml) was added thereto. The mixture was stirred at room temperature for 1 hour, and then the solvent was evaporated. The residue was dissolved in ethyl acetate, and washed successively with 1N hydrochloric acid and brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated, to give 16.0 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687664B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-b11eb93fd399418695ca779846d3ebfa |
| Source note | uspto-grants-2010_03 |