HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249844Generated: October 25, 2026
Ethyl chloroacetate → (s)-5-Ethylmorpholin-3-one
https://huagongshe.com/reaction/249844
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Amino-1-butanol, (+)- | HCID 120084 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (s)-5-Ethylmorpholin-3-one | HCID 28064773 | 88% |
Reaction Steps
To an ice cold, stirred suspension of sodium hydride (60% in oil, 1.6 g, 39.0 mmol) in toluene (50 mL) was added dropwise a solution of (S)-2-aminobutan-1-ol (1.5 g, 17.0 mmol) in toluene (36 mL). After the addition was completed, the reaction mixture was warmed to room temperature and a solution of ethyl chloroacetate (2.3 g, 19.0 mmol) in toluene (9 mL) was added in a dropwise manner. The resulting mixture was then stirred at reflux for 20 h, cooled to room temperature, and solid ammonium chloride (2.0 g, 38.7 mmol) added to the reaction. The mixture was stirred for 20 min and then concentrated under reduced pressure. The crude material was purified by column chromatography (silica gel, 95:5 CH2Cl2/CH3OH) to give (S)-5-ethylmorpholine-3-one (1.9 g, 88%) as an off-white semi-solid. 1H NMR consistent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863271B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-7b56fdd8ee294327a75f1396d93f13bd |
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| Source note | uspto-grants-2011_01 |
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