HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-(Diphenylmethyl)azetidin-3-ol | HCID 330448 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate | HCID 2758716 | — |
Reaction Steps
To a solution of 1-diphenylmethylazetidin-3-ol (see Preparation 53 (65.9 g, 275.7 mmol) in dry dichloromethane (700 ml) at 0° C. under nitrogen was added triethylamine (57 ml, 1.5 mol. equiv.). After five minutes, methanesulphonyl chloride (25.6 ml, 1.2 mol. equiv.) was added and the mixture stirred for one hour. Water (300 ml) was then added and the mixture extracted with dichloromethane (3×300 ml). The combined organic layers were dried over magnesium sulphate. The solution was then filtered and the solvent removed from the filtrate under reduced pressure. The residue was chromatographed using silica gel eluting with methanol:dichloromethane (1.49, by volume) to give the title compound (73.4 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05968923 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-91f74310cb1a4c129c9685b3f7c33c66 |
| Source note | uspto-grants-1999_10 |