HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Methanesulfonyloxymethyl-5-(3-methyl-butyryl)-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Hydroxymethyl-5-(3-methyl-butyryl)-pyridine | HCID 57656417 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Methanesulfonyloxymethyl-5-(3-methyl-butyryl)-pyridine | HCID 57656587 | 98.9% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Dissolve 2-hydroxymethyl-5-(3-methyl-butyryl)-pyridine (190 mg, 0.98 mmol) in dichloromethane (10 mL). Cool to 0° C. and add triethylamine (0.151 mL, 1.08 mmol) and methanesulfonyl chloride (0.083 mL, 1.08 mmol). Allow the mixture to warm to room temperature and stir for 2 h. Dilute the reaction mixture with dichloromethane and wash with saturated aqueous NaHCO3. Dry the organic phase over Na2SO4, filter and concentrate in vacuo to provide the title compound as oil (263 mg, 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022062B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-56f1bd56b1764cbb81f5aa48614e6ce7 |
| Source note | uspto-grants-2011_09 |