Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 58155181 | HCID 58155181 | — |
| Reactant | 38225-32-0 | HCID 86651224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58155344 | HCID 58155344 | — |
Reaction Steps
A dried flask was charged under an argon atmosphere with a solution of (R)-5-(3-bromo-phenyl)-4-(4-methoxy-benzyl)-5-methyl-morpholin-3-one (600 mg, 1.5 mmol) in tetrahydrofuran (16 ml) which was cooled to −75° C. Lithium isopropylamine (1.54 ml, 3 mmol) was added, and after the addition of diazomethane (502 mg, 3.5 mmol) the reaction was complete. For the workup, the cold reaction mixture was quenched with a saturated ammonium chloride solution (15 ml) and extracted with a mixture of dichloromethane (40 ml) and water (15 ml). The organic layer was dried over sodium sulfate and evaporated to yield the crude (2S,5R)-5-(3-bromo-phenyl)-4-(4-methoxy-benzyl)-2,5-dimethyl-morpholin-3-one as a brownish oil which was engaged in the next step without further purification. Mass (calculated) C20H22BrNO3 [404.307]; (found) [M+H]+=404, [M+2-H]+=406.
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-7832fbf9dc3d42a2854e08d10aad3b14 |
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| Source note | uspto-grants-2012_05 |
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