HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → benzyl (S)-2-(morpholin-4-yl)propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bis(2-bromoethyl) ether | HCID 21521 | — |
| Reactant | L-Alanine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1) | HCID 2802424 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | benzyl (S)-2-(morpholin-4-yl)propionate | HCID 13765076 | 66.2% |
Reaction Steps
Under an argon atmosphere, to a solution of L-alanine benzyl ester tosylate (3.4 g, 9.7 mmol) and triethylamine (6.8 ml) in dimethyl sulfoxide (17 ml) was added a solution of 1-bromo-2-(2-bromoethoxy)ethane (1.5 ml, 12 mmol) in dimethyl sulfoxide (3 ml) under ice-cooling, and the mixture was stirred at room temperature for 24 hr. To the reaction solution were added water and ethyl acetate, and the organic layer was separated. Then, the organic layer was washed with saturated brine, and dried over sodium sulfate. Sodium sulfate was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography to give the title compound (1.6 g, yield 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299070B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-7884a18d246b471885497e6efe81cae2 |
| Source note | uspto-grants-2012_10 |