HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585070Generated: October 30, 2026
Water → {2-[4-(Trifluoromethyl)phenyl]-1,3-oxazol-4-yl}methyl methylsulfonate
https://huagongshe.com/reaction/585070
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | {2-[4-(Trifluoromethyl)phenyl]-1,3-oxazol-4-yl}methanol | HCID 22064105 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {2-[4-(Trifluoromethyl)phenyl]-1,3-oxazol-4-yl}methyl methylsulfonate | HCID 22064284 | — |
Reaction Steps
A solution of {2-[4-(trifluoromethyl)phenyl]-1,3-oxazol-4-yl}methan-1-ol (0.19 g, 0.78 mmol) in tetrahydrofuran (15 ml) was cooled to 0° C., and triethylamine (0.33 ml, 2,34 mmol) was added, followed by methanesulfonyl chloride (0.12 ml, 1.56 mmol) dropwise. The mixture was stirred for 1 hour at 0° C., then water was added, and product was extracted with ethyl acetate. The organic layer was dried over sodium sulfate, and solvent removed from the filtrate under reduced pressure, to yield {2-[4-(trifluoromethyl)phenyl]-1,3-oxazol-4-yl}methyl methylsulfonate, the mesyl derivative of a compound of formula (15),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06930111B2 |
|---|
| Source dataset | uspto-grants-2005_08 |
|---|
| ORD ID | ord-04ca0f5b35e04a0f9e85ec7e3f581f18 |
|---|
| Source note | uspto-grants-2005_08 |
|---|