HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374977Generated: October 31, 2026
Ethyl Acetate → (3R)-4-(2-chloroethyl)-3-(methoxymethyl)morpholine hydrochloride
https://huagongshe.com/reaction/1374977
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-methoxymethylmorpholino]ethanol (505 mg) in toluene (2.5 ml) was added dropwise a solution of thionyl chloride (429 mg) in toluene (1.5 ml) below 5° C. under nitrogen atmosphere. The mixture was stirred at 70° C. for 1.5 hours. After the mixture was cooled at room temperature, ethyl acetate was added to the mixture, and resulting suspension was evaporated under reduced pressure. Diisopropyl ether was added to the residue, and after the mixture was stirred at room temperature for 15 minutes, the resulting precipitates were collected by filtration, washed with diisopropyl ether and dried at 40° C. under reduced pressure to give (3R)-4-(2-chloroethyl)-3-(methoxymethyl)morpholine hydrochloride (620 mg) as a light yellowish powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166598B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-465d11a10cf44283a467a7ddea70331d |
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| Source note | uspto-grants-2007_01 |
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