HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (1-Benzhydrylazetidin-3-yl)methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (1-Benzhydrylazetidin-3-yl)methanol | HCID 2758715 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1-Benzhydrylazetidin-3-yl)methyl methanesulfonate | HCID 21978370 | 99% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
The title compound from Step B above (1.7 g, 6.72 mmoles) and triethylamine (1.1 g, 10.87 mmoles) were dissolved in CH2Cl2 (20 mL) and the mixture was stirred under nitrogen at 0° C. Methanesulfonylchloride (1.1 g, 9.6 mmoles) was added and the solution was stirred at room temperature for 2 h. The solution was diluted with CH2Cl2 and washed with saturated aqueous sodium bicarbonate, water and dried (MgSO4), filtered and evaporated to dryness to give the title compound (2.32 g, 99%). FABMS (M+1)=332.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06800636B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-be4167c7ed454984976d4cd793f7cd00 |
| Source note | uspto-grants-2004_10 |