HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → (3,3-Difluoro-1-methylcyclobutyl)methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (3,3-Difluoro-1-methyl-cyclobutyl)methanol | HCID 58564885 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3,3-Difluoro-1-methylcyclobutyl)methyl methanesulfonate | HCID 118061633 | 63.5% |
Reaction Steps
To a solution of Intermediate 229A (100 mg, 0.735 mmol) and TEA (0.102 mL, 0.735 mmol) in DCM was added methanesulfonyl chloride (0.059 mL, 0.735 mmol) dropwise at 5° C. and the reaction mixture was stirred for 3 h. The reaction mass was diluted with DCM, washed with water and brine, dried over Na2SO4, filtered and the filtrate evaporated under reduced pressure. The crude product was purified by silica gel chromatography (12 g REDISEP® column, eluting with 30% EtOAc in petroleum ether). Fractions containing the product were combined and evaporated to afford the Intermediate 229B as a yellow oil (100 mg, 63.5%). 1H NMR (400 MHz, DMSO-d6) δ ppm 4.27 (s, 2H), 3.01 (s, 3H), 2.55-2.69 (m, 2H), 2.06-2.37 (m, 2H), 1.15 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273058B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-31dfc2be8e0e4233bc1807a97cb3f30d |
| Source note | uspto-grants-2016_03 |