Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Ethyl 3-ethoxy-3-iminopropionate hydrochloride | HCID 75345 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90093768 | HCID 90093768 | 70.6% |
Reaction Steps
Ethyl 3-Ethoxy-3-iminopropanoate Hydrochloride (Preparation 118, 50 g, 0.256 mol) was suspended in dichloromethane (600 mL). The suspension was cooled to −15° C. and triethylamine (7.8 mL, 0.56 mol) followed by pivaloyl chloride (31.5 mL, 0.256 mol) were added. The reaction mixture was left for 18 hours at room temperature, then washed with water, dried over MgSO4, and evaporated. The residue was triturated with hexane. The resulting precipitate was filtered and dried to afford the title compound (44 g, 70%). Taken directly on to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09163021B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-a501077e27a9423eaeb43fe34d9588f5 |
|---|
| Source note | uspto-grants-2015_10 |
|---|