HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl bromoacetate → [tert-Butoxycarbonyl-(3,4-difluorophenyl)-amino]-acetic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Carbamic acid, (3,4-difluorophenyl)-, 1,1-dimethylethyl ester | HCID 2783369 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [tert-Butoxycarbonyl-(3,4-difluorophenyl)-amino]-acetic acid methyl ester | HCID 54030684 | — |
Reaction Steps
To a solution of (3,4-difluorophenyl)-carbamic acid tert-butyl ester (Tetrahedron, (1992), 48(35), 7373) (15.1 g) in tetrahydrofuran (120 ml) at 0° C. was added potassium tert-butoxide (94 ml of a 1.0 M solution in tetrahydrofuran) dropwise. After stirring for 2 hr methyl bromoacetate (9.1 ml) was added dropwise and ice-bath removed and reaction mixture stirred at room temperature overnight. Reaction mixture concentrated under reduced pressure, diluted with ethyl acetate and washed with water and brine, dried (Na2SO4) and concentrated to leave the sub-title compound as a brown oil (18.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06555541B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-302bd5a608e94b5ca6ff9967c6d1887a |
| Source note | uspto-grants-2003_04 |