HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-BOC-3(R)-methylsulfonyloxymethyl-piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | tert-butyl (3R)-3-(hydroxymethyl)piperidine-1-carboxylate | HCID 1514447 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-BOC-3(R)-methylsulfonyloxymethyl-piperidine | HCID 10108453 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
2.16 ml of methanesulphonyl chloride followed by 3.86 ml of triethylamine are added to a solution of 5 g of (R)-3-hydroxymethylpiperidine-1-carboxylic acid tert-butyl ester in 80 ml of DCM cooled to 0° C. The medium is stirred at 0° C. for 1 h 30 min and 0.7 ml of triethylamine and 0.54 ml of methanesulphonyl chloride are again added. After 30 min at 0° C., the medium is hydrolysed, and the organic phase is washed twice in water and then with a saturated NaCl solution, and then dried over MgSO4. The medium is evaporated, to give 6.8 g of a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07767681B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-f0d21d91905148a0af67c3a60fc88b44 |
| Source note | uspto-grants-2010_08 |