HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → HCID 54195487, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Reactant | Methyl valinate hydrochloride | HCID 111190 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 54195487 | HCID 54195487 | 22% |
Reaction Steps
A solution of 2.12 g (12.6 mmol) of L-valine methyl ester hydrochloride, 2.0 ml (12.6 mmol) of benzyl bromoacetate, and 3.5 ml (31 mmol) of 4-methylmorpholine in 100 ml of dioxane was heated at reflux for 4 h. After being allowed to cool, the solution was concentrated in vacuo and partitioned between ether and water. The organic layer was dried over MgSO4 and concentrated in vacuo. Chromatography on silica gel using 20% ethyl acetate in hexane provided 0.77 g (22%) of the desired compound as a colorless oil (Rf 0.24, 20% ethyl acetate in hexane. 1H NMR δ 0.95 (d, J=7 Hz, 6H), 1.96 (br, 1H), 1.98 (octet, J=7 Hz, 1H), 3.08 (d, J=6 Hz, 1H), 3.43 (AA', 2H), 3.71 (s, 3H), 5.16 (s, 2H), 7.36 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05142056 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-f9444f041a844c8caa5b145cd2a0dd71 |
| Source note | uspto-grants-1992_08 |