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Methyl iodide → HCID 58155245, compound

HRID 1929492
Notes
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Reaction equation

HRID 1929492 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([C@@:8]2([CH3:25])[N:13]([CH2:14][C:15]3[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=3)[C:12](=[O:23])[C@H:11]([CH3:24])[O:10][CH2:9]2)[CH:5]=[CH:6][CH:7]=1.[CH:26]([N-]C(C)C)(C)C.[Li+].IC>O1CCCC1>[Br:1][C:2]1[CH:3]=[C:4]([C@@:8]2([CH3:25])[N:13]([CH2:14][C:15]3[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=3)[C:12](=[O:23])[C:11]([CH3:26])([CH3:24])[O:10][CH2:9]2)[CH:5]=[CH:6][CH:7]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 2724682Lithium diisopropylamideHCID 58155344HCID 58155344, compound

Product 1

HCID 58155245HCID 58155245, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-75 °C

Procedure

A dried flask was charged under an argon atmosphere with a solution of the crude (2S,5R)-5-(3-bromo-phenyl)-4-(4-methoxy-benzyl)-2,5-dimethyl-morpholin-3-one (622 mg) in tetrahydrofuran (16 ml) which was cooled to −75° C. Lithium diisopropylamide (1.54 ml, 3 mmol) was rapidly added, followed by iodomethane (502 mg, 3.5 mmol). After 15 minutes at −75° C. 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. The crude product was purified by chromatography on silica gel using a gradient of heptane and ethyl acetate=100/0 to 66/34 as the eluent. The (R)-5-(3-bromo-phenyl)-4-(4-methoxy-benzyl)-2,2,5-trimethyl-morpholin-3-one was obtained as a white solid (495 mg, 77% of theory). Mass (calculated) C21H24BrNO3 [418.334]; (found) [M+H]+=418, [M+2-H]+=420.

Workup

  1. customFor the workup, the cold reaction mixture
  2. customwas quenched with a saturated ammonium chloride solution (15 ml)
  3. extractionextracted with a mixture of dichloromethane (40 ml) and water (15 ml)
  4. dry with materialThe organic layer was dried over sodium sulfate
  5. customevaporated
  6. customThe crude product was purified by chromatography on silica gel using a gradient of heptane and ethyl acetate=100/0 to 66/34 as the eluent

Sources & evidence

ORD record
ord-521a0bdf87c643e6b324c393fd3c0c41
Source dataset
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08188079B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes