HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

2H-1,4-Benzoxazin-3(4H)-one,4-methyl- → 2H-1,4-Benzoxazine, 3,4-dihydro-4-methyl-

HRID 72558
Notes
Print preview

Reaction equation

HRID 72558 reaction equation
[CH3:1][N:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[O:5][CH2:4][C:3]1=O>C1COCC1>[CH3:1][N:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[O:5][CH2:4][CH2:3]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 890322H-1,4-Benzoxazin-3(4H)-one,4-methyl-

Product 1

HCID 37550242H-1,4-Benzoxazine, 3,4-dihydro-4-methyl-Yield 100.3%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a stirred solution of 4-methyl-4H-benzo[1,4]oxazin-3-one (2.18 g, 13.37 mmol) in THF (5 mL) was added borane-tetrahydrofuran complex (4.02 g, 46.8 mmol) at room temperature. After stirring the solution for 2 h, the reaction mixture was refluxed for 4 h. After complete conversion, reaction mixture was quenched by adding MeOH (10 mL) and evaporated the solvents. The residue obtained was extracted with ethyl acetate (30×2 mL) and the organic layer was washed with water (20 mL), brine (20 mL) and evaporation of solvent gave 4-methyl-3,4-dihydro-2H-benzo[1,4]oxazine 2.0 g.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • temperaturethe reaction mixture was refluxed for 4 h
  • customAfter complete conversion, reaction mixture
  • customwas quenched
  • additionby adding MeOH (10 mL)
  • customevaporated the solvents
  • customThe residue obtained
  • extractionwas extracted with ethyl acetate (30×2 mL)
  • washthe organic layer was washed with water (20 mL), brine (20 mL) and evaporation of solvent
  • Sources & evidence

    ORD record
    ord-0165b565e08449a89ac8f06d349cbf4e
    Source dataset
    uspto-grants-2014_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08828951B2

    Reaction notes

    Loading…