HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → Benzyl trans-3-azido-4-fluoro-pyrrolidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (trans)-3-Azido-4-fluoropyrrolidine | HCID 118073556 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl trans-3-azido-4-fluoro-pyrrolidine-1-carboxylate | HCID 57970079 | 100% |
Reaction Steps
To a stirred mixture of (trans)-3-azido-4-fluoropyrrolidine (18 g) in CH2Cl2 (120 mL) was added DIPEA (35 g, 0.27 mol, 2.5 eq), then CBZ-Cl (22 g, 0.13 mol) was added dropwise at 0-5° C. After addition, the resulting mixture was stirred at rt overnight. The mixture was washed with sat. aq. NH4Cl (150 mL), sat. aq. NaHCO3 (3×40 mL) and brine (40 mL). The organic layer was concentrated and purified by column (petroleum ether/EtOAc=10:1˜5:1) to give the title compound (30 g, ˜100% yield in two steps, containing residual EtOAc and DCM) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290496B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-76613ed904d642f18b18e108a99a5b4f |
| Source note | uspto-grants-2016_03 |