HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → Benzyl N-methyl-N-(2-oxoethyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-Cbz-N-methyl-2-aminoethanol | HCID 13279869 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl N-methyl-N-(2-oxoethyl)carbamate | HCID 12010768 | 100% |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
DMSO (71 mL, 1 mol) and DIPEA (87.1 mL, 0.5 mol) were added to a stirred solution of the product of step (a) (20.9 g, 0.1 mol) in dichloromethane (200 mL) at −10° C. The reaction mixture was stirred at −10° C. for 15 min and then sulfur trioxide pyridine complex (79.6 g, 0.5 mol) was added and the resulting mixture was stirred for 1 hour. The reaction mixture was quenched with addition of 1 M hydrochloric acid (200 mL). The organic layer was separated and washed with saturated aqueous sodium bicarbonate (100mL), brine (100 mL), dried (potassium carbonate) and solvent removed under reduced pressure to give the title compound (20.7 g, ˜100% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514558B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-e9479ec0a564461b85aed86ab982c2c8 |
| Source note | uspto-grants-2009_04 |