HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Boc-(R)-alpha-(4-bromobenzyl)proline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-(tert-butoxycarbonyl)-2-(4-bromobenzyl)proline ethyl ester | HCID 69212228 | — |
| Solvent | Water | HCID 962 | — |
| Product | Boc-(R)-alpha-(4-bromobenzyl)proline | HCID 2761850 | 108% |
Reaction Steps
A mixture of N-(tert-butoxycarbonyl)-2-(4-bromobenzyl)proline ethyl ester (3.00 g), LiOH (10 mmol), THF (25 mL), MeOH (10 mL) and H2O (5 mL) was stirred at room temperature overnight. The mixture was then heated at 74° C. overnight. The mixture was concentrated in vacuo, and water was added. The mixture was washed with Et2O and the aqueous layer was made acidic with the addition of 1N H2SO4. The aqueous layer was extracted with EtOAc. The EtOAc layer was washed with brine, dried over Na2SO4, and evaporated to give N-(tert-butoxycarbonyl)-2-(4-bromobenzyl)proline (3.02 g). MS (m/z) 284 (MH+-t-Boc); mp: 143.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06897225B1 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-76ba3c8e568549a2809cf05b71b54723 |
| Source note | uspto-grants-2005_05 |