HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-[5-(3-Cyanophenyl)-1-benzofuran-2-yl]ethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-[2-(2-Hydroxyethyl)-1-benzofuran-5-yl]benzonitrile | HCID 11414365 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[5-(3-Cyanophenyl)-1-benzofuran-2-yl]ethyl methanesulfonate | HCID 22274445 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
The product from Example 112C (170 mg, 0.65 mmol) and triethylamine (100 μL, 0.72 mmol) were dissolved into CH2Cl2 (3 mL) and cooled to 0° C. The solution was treated with methanesulfonyl chloride (55 μL, 0.71 mmol), and after 10 minutes it was permitted to slowly warm to room temperature. More methanesulfonyl chloride (10 μL, 0.13 mmol) and triethylamine (10 μL, 0.072 mmol) were added. The mixture was stirred until the reaction was nearly complete and then washed consecutively with water and brine, dried (Na2SO4), concentrated, and used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538138B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-23cb2fec81b44a0399efa54afcdf71fe |
| Source note | uspto-grants-2009_05 |