HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(1-Pyrrolyl)benzyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | [3-(1H-Pyrrol-1-yl)phenyl]methanol | HCID 2776531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(1-Pyrrolyl)benzyl methanesulfonate | HCID 19744531 | 93.3% |
Reaction Steps
170 mg of the resulting alcohol compound was dissolved in 10 ml of methylene chloride, and 120 mg of methanesulfonyl chloride and 150 mg of triethylamine were added. The mixture was stirred for 1 hour under ice cooling. The reaction mixture was washed with water, and dried over anhydrous magnesium sulfate. The solvent was evaporated to give 230 mg (yield 92%) of the captioned compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05234946 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-df63b00ecffe444bbbaf046c5204bea7 |
| Source note | uspto-grants-1993_08 |