HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 57429671, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 57429670 | HCID 57429670 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57429671 | HCID 57429671 | 75.1% |
Reaction Steps
To a mixture of solution of [5-(4-Fluoro-benzyl)-4,5-dihydro-isoxazol-3-yl]-methanol (80 mg, 0.38 mmol), TEA (57 mg, 0.57 mmol) in DCM (10 ml), methanesulfonyl chloride (43 mg, 0.38 mmol) was added slowly at 0° C. and the mixture was stirred at room temperature for 3 hrs. Aqueous NaHCO3 was added to the reaction mixture and extracted with methylene dichloride. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated under vacuum. The residue obtained was purified by column chromatography to obtain Methanesulfonic acid 5-(4-fluoro-benzyl)-4,5-dihydro-isoxazol-3-ylmethyl ester (82 mg, 75%) as brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08252797B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-f0d58c1cceec462dafc54e176a6b04ce |
| Source note | uspto-grants-2012_08 |