HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl oxoacetate → Ethyl 2-((tert-butylsulfinyl)imino)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-((tert-butylsulfinyl)imino)acetate | HCID 72998703 | — |
Reaction Steps
A mixture of ethyl 2-oxoacetate (50% solution in toluene; 4.066 g; 20.00 mmol), 2-methylpropane-2-sulfinamide (2.424 g; 20.00 mmol), and 4 angstrom molecular sieves (60 g) in anh. DCM (250 ml) was stirred at rt, under nitrogen, for 65 h. The reaction mixture was then filtered over celite, and the separated solids were washed with AcOEt (3×200 ml). The filtrate was then dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure affording ethyl 2-((tert-butylsulfinyl)imino)acetate as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242970B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-e539e16197a64c259698f93b40129b4d |
| Source note | uspto-grants-2016_01 |