HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfide → HCID 57788115, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 10967413 | HCID 10967413 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57788115 | HCID 57788115 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To (R)-methyl 2-(tert-butoxycarbonylamino)-2-phenylacetate (E4) in DMF at −40° C. was added NaH and the solution was warmed to 0° C. for 20 minutes. DMS was added and solution was stirred at room temperature for 3 hours. The mixture was poured into NH4Cl(sat)/HCl (1N) 3:1 and extracted with EtOAc. The organics were dried (Na2SO4), filtered and evaporated to give crude E5. Column chromatography Hexanes/EtOAc gave pure (R)-methyl 2-(tert-butoxycarbonyl(methyl)amino)-2-phenylacetate (E5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871757B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-2a28413f1dfc4fd59d2f5715de02eecf |
| Source note | uspto-grants-2014_10 |