HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424435Generated: October 30, 2026
Chloroacetyl chloride → HCID 86630238, compound
https://huagongshe.com/reaction/424435
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 86630236 | HCID 86630236 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 86630238 | HCID 86630238 | 100% |
Reaction Steps
Chloroacetyl chloride (27.5 g, 243 mmol) was dropped to a solution of 4-((1S)-2-benzylamino-1-hydroxyethyl)phenyl methanesulfonate (71 g, 221 mmol) in 1N aqueous sodium hydroxide (330 ml) and stirred for one hour at room temperature. Resulting solution was extracted with chloroform, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. Potassium hydroxide (85%, 17.5 g, 265 mmol) was added to a solution of the resulting pale brown oil in 2-propanol (600 ml), and the mixture was stirred for 10 hours. The solvent was removed in vacuo and the residue was partitioned between water and chloroform. The organic layer was washed with 0.5 M hydrochloric acid, saturated sodium hydrogen carbonate, brine and dried over anhydrous magnesium sulfate. Removal of the solvent under reduced pressure furnished 4-((2S)-4-benzyl-5-oxo-morpholin-2-yl)phenyl methanesulfonate (79.8 g, 100%) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106045B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-4991c66c0a0f45a5bea2e7619dd7ad87 |
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| Source note | uspto-grants-2012_01 |
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