HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349905Generated: October 30, 2026
Triethylamine → 2-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)phenyl]ethyl methanesulfonate
https://huagongshe.com/reaction/349905
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)phenyl]ethan-1-ol | HCID 69172077 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)phenyl]ethyl methanesulfonate | HCID 86760416 | 96.3% |
Reaction Steps
Methanesulfonyl chloride (3.37 g) was added dropwise to a mixture of 2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]ethan-1-ol (7.0 g), triethylamine (2.97 g), and ethyl acetate (300 ml) at 0° C., and the mixture was stirred for 3 hours at room temperature. The reaction mixture was poured into water, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium bicarbonate, 1N hydrochloric acid and then with saturated aqueous sodium chloride solution, then dried (MgSO4), and concentrated. The crystals obtained were collected by filtration to yield 2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]ethyl methanesulfonate (8.44 g, yield: 96%). This was recrystallized from ethyl acetate-hexane. Melting point: 66–67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07179823B1 |
|---|
| Source dataset | uspto-grants-2007_02 |
|---|
| ORD ID | ord-c3290d0df06b457797acaa0291625be1 |
|---|
| Source note | uspto-grants-2007_02 |
|---|