HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → benzyl (S)-1-tert-butoxycarbonylpyrrolidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | (3S)-1-[(tert-butoxy)carbonyl]pyrrolidine-3-carboxylic acid | HCID 1512492 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | benzyl (S)-1-tert-butoxycarbonylpyrrolidine-3-carboxylate | HCID 59016658 | — |
Reaction Steps
DBU (0.764 mL) was added to a mixture of benzyl bromide (0.61 mL), (S)-1-tert-butoxycarbonyl-pyrrolidine-3-carboxylic acid (1 g) in anhydrous toluene (10 mL) and the mixture was stirred at room temperature for 24 hours. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-35% to give benzyl (S)-1-tert-butoxycarbonylpyrrolidine-3-carboxylate (0.859 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290472B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-68de794ff3c6415c8404db350a5cfa37 |
| Source note | uspto-grants-2016_03 |