HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593335Generated: October 26, 2026
Methanol → 5-(3-Bromophenyl)-5-methylmorpholin-3-one
https://huagongshe.com/reaction/593335
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| 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 tert-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. 4.18 g (88%) of (RS)-5-(3-bromo-phenyl)-5-methyl-morpholin-3-one were obtained as a white solid. Mass (calculated) C11H12BrNO2 [270.128]; (found) [M+H]+=270 and [M+2+H]+=272.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09242943B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-a21957b6e82846cea0a987a0688435e0 |
|---|
| Source note | uspto-grants-2016_01 |
|---|