HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-methyl-2-(4-nitro-1H-pyrazol-1-yl)propyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Methyl-2-(4-nitro-pyrazol-1-yl)-propan-1-ol | HCID 117840940 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-methyl-2-(4-nitro-1H-pyrazol-1-yl)propyl methanesulfonate | HCID 117840921 | — |
Reaction Steps
To a solution of 2-methyl-2-(4-nitro-1H-pyrazol-1-yl)propan-1-ol (13 g) obtained in Step G of Example 103 in tetrahydrofuran (100 mL) were added successively dropwise triethylamine (12 mL) and methanesulfonyl chloride (6.3 mL) at 0° C. under nitrogen atmosphere, and the mixture was stirred at room temperature for 2 hr. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the crude title compound (18 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187453B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-9b95c9f84a2a415a95425145cf7c46d1 |
| Source note | uspto-grants-2015_11 |