HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (R)-2-((tert-butoxycarbonyl)amino)propyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | tert-butyl N-((2R)-1-hydroxypropan-2-yl)carbamate | HCID 13200309 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-2-((tert-butoxycarbonyl)amino)propyl methanesulfonate | HCID 14427185 | — |
Reaction Steps
Methanesulfonyl chloride (0.64 mL) was added dropwise to an ice-cooled mixture of (R)-(+)-2-(tert-butoxycarbonylamino)-propanol (1.31 g) and triethylamine (1.6 mL) in methylene chloride (20 mL) with stirring, and the mixture was stirred at that temperature for 1 hr. The reaction mixture was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford the title compound (1.93 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07417169B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-fcaba5752dee4b9ea0c3b341aba2b82f |
| Source note | uspto-grants-2008_08 |