HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765984Generated: November 1, 2026
Ethyl Acetate → (3R)-4-(2-chloroethyl)-3-(methoxymethyl)morpholine hydrochloride
https://huagongshe.com/reaction/1765984
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-[(3R)-3-methoxymethylmorpholino]ethanol | HCID 53827486 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (3R)-4-(2-chloroethyl)-3-(methoxymethyl)morpholine hydrochloride | HCID 69331387 | 149.4% |
Reaction Steps
To an ice-cooled solution of 2-[(3R)-3-(methoxy-methyl)morpholino]ethanol (505 mg) in toluene (2.5 ml) was added dropwise a solution of thionyl chloride (429 mg) in toluene (1.5 ml) at 5° C. or below under a nitrogen atmosphere. The mixture was stirred at 70° C. for 1.5 hours. After cooling the mixture to room temperature, ethyl acetate was added to the mixture and the solvent was evaporated from the produced suspension under reduced pressure. Diisopropyl ether was added to the residue. After stirring the mixture at room temperature for 15 minutes, the produced precipitates were filtered, washed with diisopropyl ether and dried at 40° C. under reduced pressure to give (3R)-4-(2-chloroethyl)-3-(methoxymethyl)morpholine hydrochloride (620 mg) in the form of pale yellow powders.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07229992B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-b0681da4b5424b4ea0da8c9d843d19b5 |
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| Source note | uspto-grants-2007_06 |
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