HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → 3-allyloxycarbonylamino-N-methoxy-N-methyl-succinamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-Allyloxycarbonylamino-succinic acid 4-tert-butyl ester | HCID 23598659 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-allyloxycarbonylamino-N-methoxy-N-methyl-succinamic acid tert-butyl ester | HCID 23598711 | 81% |
Reaction Steps
2-Allyloxycarbonylamino-succinic acid 4-tert-butyl ester, 100, (43.4 g, 0.159 mol) is dissolved in CH2Cl2(900 mL). To this solution O,N-dimethyl-hydroxylamine hydrochloride (18.6 g, 0.191 mol), 4-Methyl-morpholine (21.0 mL, 19.3 g, 0.191 mol), and 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (36.6 g, 0.191 mol) are added. After the consumption of the starting material, the solution is washed with 1.0 N HCl (2×400 mL) and brine (1×250 mL). The organic layer is concentrated in vacuo and the residue purified over silica (hexanes/ethyl acetate 65:35) to afford 40.8 g (81% yield) of the desired product as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07001899B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-776448b980944401919c3e344cfc54eb |
| Source note | uspto-grants-2006_02 |