HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929457Generated: October 25, 2026
Methanol → 5-(3-Bromophenyl)-5-methylmorpholin-3-one
https://huagongshe.com/reaction/1929457
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Butylate | HCID 16181 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | N-[1-(3-Bromophenyl)-2-hydroxy-1-methylethyl]-2-chloroacetamide | HCID 58155284 | — |
| Solvent | 2-Methyl-2-butanol | HCID 6405 | — |
| Product | 5-(3-Bromophenyl)-5-methylmorpholin-3-one | HCID 58155305 | 91% |
Reaction Steps
A solution of (RS)-N-[1-(3-bromo-phenyl)-2-hydroxy-1-methyl-ethyl]-2-chloro-acetamide (5.36 g, 17 mmol) in 2-methyl-2-butanol (100 ml) was treated in one portion with potassium tent-butylate (6.66 g, 58 mmol). Initially, the temperature rose to 30° C.; the reaction mixture was left to cool to room temperature and stirring was continued for one hour. For the workup, the reaction mixture was treated with methanol (50 ml), then evaporated at reduced pressure. The residue was purified by chromatography on silica gel using a gradient of dichloromethane/methanol=100/0 to 75/25 as the eluent. There were obtained 4.18 g (88% of theory) of (RS)-5-(3-bromo-phenyl)-5-methyl-morpholin-3-one as a white solid. Mass (calculated) C11H12BrNO2 [270.128]; (found) [M+H]+=270, [M+2-H]+==272.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188079B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-4b4d45f8e75542c4ab3273f779f65774 |
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| Source note | uspto-grants-2012_05 |
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