HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Pyrrolidinol, 1-(phenylmethyl)-, 3-methanesulfonate, (3R)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (R)-(+)-1-Benzyl-3-pyrrolidinol | HCID 643472 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Pyrrolidinol, 1-(phenylmethyl)-, 3-methanesulfonate, (3R)- | HCID 11807254 | — |
Reaction Steps
10 g of (R)-1-(phenylmethyl)-3-pyrrolidinol were dissolved in 160 ml of anhydrous toluene. The solution was stirred under a stream of nitrogen, cooled in an ice/ethanol bath and 8.7 ml of triethylamine were added. At a temperature of −5° C. 4,9 ml of a solution of methanesulfonylchloride in 110 ml of anhydrous toluene were added dropwise over 1,5 hours and the reaction mixture was stirred for 1 hour at 0° C. The solid was filtered and washed with ethyl acetate. The filtrate was washed with water, dried and evaporated in vacuo to give 13,9 g of (R)-3-methanesulfonyloxy-1-(phenylmethyl)-pyrrolidine as an almost colourless oil. M.S. (C.I.) (M/Z): 256 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06281243B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-800ffe8253774ac6b84901fe7fe031e9 |
| Source note | uspto-grants-2001_08 |