HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → (S)-1-(tetrahydrofuran-2-yl)methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (2S)-(+)-2-(Hydroxymethyl)tetrahydrofuran | HCID 637528 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (S)-1-(tetrahydrofuran-2-yl)methyl methanesulfonate | HCID 18649743 | — |
Reaction Steps
Mesylchloride (12.1 g) was added to a mixture of (S)-1-(Tetrahydro-furan-2-yl)-methanol (10.0 g) and pyridine (55 mL) at −15° C. and stirred for 1.5 hours at room temperature. The mixture was poured into ice water and extracted with ethyl acetate. The organic phase was washed with a solution of potassium hydrogensulfate (20%) and with a solution of saturated sodium hydrogencarbonate, dried over magnesium sulfate and concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822495B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-c239c99e0dac47eabc6971ad83b5e709 |
| Source note | uspto-grants-2014_09 |