HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,2-Difluoropropane-1,3-diyl dimethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2,2-Difluoropropane-1,3-diol | HCID 95744 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Difluoropropane-1,3-diyl dimethanesulfonate | HCID 242871 | 84% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 5 g (44.6 mmol) 2,2-difluoropropane-1,3-diol (prepared as described in J. Med. Chem. 1994, 37, 1857-1864) in DCM (50 mL) was added triethylamine (18.6 mL, 133.83 mmol) and methane sulphonyl chloride (6.9 mL, 89.22 mmol) at 0° C. and stirred for 1 h at 0° C. Thereafter the reaction mixture was quenched with water and extracted with DCM. The organic layer was dried over anhydrous sodium sulphate and concentrated to afford 2,2-difluoropropane-1,3-diyl dimethanesulfonate (9 g, 84%) which was used immediately in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023844B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-6897520d27f9497e907addb4497dad07 |
| Source note | uspto-grants-2015_05 |