HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → 3-Tosyl-Cbz-(R)-Pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (R)-(-)-1-CBZ-3-pyrrolidinol | HCID 11183628 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Tosyl-Cbz-(R)-Pyrrolidine | HCID 67182709 | 94.6% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
3-Hydroxy-Cbz-(R)-pyrrolidine (13.7 g, 0.06 mol) was dissolved in CH2Cl2 (250 mL) and cooled to 0° C. p-Toluenesulfonyl chloride (14.16 g, 0.07 mol), and triethylamine (20.7 mL, 0.15 mol) were added and the resulting solution was stirred for 4 h at 0° C. The solution was washed with 1 M HCl, saturated NaHCO3, and brine. The organic solution was dried over MgSO4 and concentrated. The crude product was purified by column chromatography eluting with ethyl acetate/hexanes (3/1, v/v) to afford 20.4 g (88% yield) of the desired product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06914048B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-303bb7014bee4595b7b015b581e3afa7 |
| Source note | uspto-grants-2005_07 |