HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → HCID 54368637, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | HCID 10468399 | HCID 10468399 | — |
| Reactant | HCID 131717593 | HCID 131717593 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 54368637 | HCID 54368637 | — |
Reaction Steps
11.1 g of Ala-Oic-OBzl.TFA, 7 g of α-bromophenylbutyric acid ethyl ester and 3.3 ml of N-ethylmorpholine are stirred in 20 ml of dimethylacetamide for 4 days at room temperature. The mixture is concentrated to a large extent in vacuo, the residue is dissolved in methanol, the methanolic solution is adjusted to pH 2 with aqueous 2N HCl, and lipophilic compounds are extracted with petroleum ether. The methanolic phase is concentrated and 5% sodium carbonate solution is added to it, and the reaction product is extracted in ethyl acetate. Chromatography over silica gel (system ethyl acetate/petroleum ether 5:3) yields the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05158959 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-dd1e76a2ff954674a8d0478073dfcb90 |
| Source note | uspto-grants-1992_10 |