HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxyethanol → HCID 22273536, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxyethanol | HCID 8019 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | HCID 22273469 | HCID 22273469 | — |
| Reactant | 2-Methoxyethyl trifluoromethanesulfonate | HCID 22273493 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22273536 | HCID 22273536 | — |
Reaction Steps
A solution of 2-methoxyethyl triflate (prepared on a 6 mmole scale from 2-methoxyethanol and trifluoromethanesulphonic anhydride by the method published in Synthesis 1982 85) in DCM (20 ml) was added dropwise to a solution of 1-(triphenylmethyl)-2-methyl-4-acetylimidazole (Method 34; 1.5 g, 4 mmol) in DCM (5 ml) and the mixture was stirred for 40 hours at ambient temperature. The volatiles were removed by evaporation to give a solid (2.4 g) which was purified by flash chromatography on silica gel eluting with DCM/MeOH (100:0 increasing in polarity to 95:5) to yield the title compound (660 mg, 88%) as a solid NMR (CDCl3) 1.31 (s, 3H), 1.49 (s, 3H), 2.02 (s, 3H), 2.43 (m, 2H), 3.31 (m, 2H), 6.87 (s, 1H); m/z 183.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06969714B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-234fd86570c4499c9b313709d13e6df4 |
| Source note | uspto-grants-2005_11 |