HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Glycine, N-[2-(methylsulfonyl)ethyl]-N-(trifluoroacetyl)-, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22609710 | HCID 22609710 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Glycine, N-[2-(methylsulfonyl)ethyl]-N-(trifluoroacetyl)-, ethyl ester | HCID 22609755 | 90% |
Reaction Steps
Sodium hydride (60% dispersion in mineral oil, 0.190 g, 4.75 mmol) was added to a solution of N-(2-methylsulphonylethyl)trifluoroacetamide (0.986 g, 4.50 mmol) in dry DMF (10 ml) and the mixture was stirred under a nitrogen atmosphere for 30 minutes. Ethyl bromoacetate (0.55 ml, 0.828 g, 4.96 mmol) was added and the mixture was stirred at room temperature overnight. The mixture was poured into ice-water, and extracted with ethyl acetate. This solution was washed with water, dried (MgSO4), and concentrated in vacuo to give the title compound as a white solid (1.239 g, 4.03 mmol, 90%); δH CDCl3 4.17 (4H,m), 3.91 (2H,t), 3.46 (2H,t), 2.98 (3H,s), 1.30 (3H,t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06391874B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-2557300afaf245e2b9e53dfbd46f0fa6 |
| Source note | uspto-grants-2002_05 |