HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Tert-butyl 2-[(methanesulfonyloxy)methyl]pyrrolidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | tert-Butyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate | HCID 550865 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 2-[(methanesulfonyloxy)methyl]pyrrolidine-1-carboxylate | HCID 18007568 | — |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
To a solution of tert-butyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate (1.0 g, 5.0 mmol) and TEA (1.0 g, 9.9 mmol) in CH2Cl2 (40 mL) was slowly added MsCl (0.63 g, 5.5 mmol). The reaction mixture was stirred for 30 min at −20° C. and then water (60 mL) was added. The aqueous phase was separated and extracted with CH2Cl2. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to afford the crude tert-butyl 2-((methylsulfonyloxy)methyl)pyrrolidine-1-carboxylate that was used directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126940B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-e99034a380a54f8c9f06edbf84196867 |
| Source note | uspto-grants-2015_09 |