Water → 5-methyl-1H-benzo[d][1,3]oxazin-2(4H)-one

HRID 1387258Notes

Reaction equation

HRID 1387258 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[CH2:9][OH:10].C(N(CC)CC)C.[C:18](Cl)(Cl)=[O:19].O>C1COCC1.CCOC(C)=O>[CH3:8][C:4]1[C:3]2[CH2:9][O:10][C:18](=[O:19])[NH:1][C:2]=2[CH:7]=[CH:6][CH:5]=1

Participants

7

Reactant 4

HCID 962WaterHCID 6371PhosgeneHCID 8471TriethylamineHCID 15339417(2-Amino-6-methylphenyl)methanol

Product 1

HCID 105589525-methyl-1H-benzo[d][1,3]oxazin-2(4H)-one

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolventHCID 8857Ethyl AcetateSolvent

Procedure

To a solution of (2-amino-6-methyl-phenyl)-methanol (2.74 g, 20 mmol) and triethylamine (4.04 g, 40 mmol) in THF (150 mL), phosgene (12.5% solution in toluene, 17.42 g, 22 mmol) was added dropwise at 0° C. Reaction mixture was allowed to warm to room temperature and stirred for 16 hours. Water (150 mL) was added under stirring, followed by EtOAc (2×100 mL). EtOAc extracts were washed with water and brine and dried over MgSO4. The product (buff solid) was crystallized from EtOAc:pet. ether mixture.

Workup

  1. customReaction mixture
  2. stirringunder stirring
  3. washEtOAc extracts were washed with water and brine
  4. dry with materialdried over MgSO4
  5. customThe product (buff solid) was crystallized from EtOAc

Sources & evidence

ORD record
ord-4b466c5813f5432898eacbaec7841dac
Source dataset
uspto-grants-2001_07
Patent number
US06268366B1

Reaction notes

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