Identification | Back Directory | [Name]
6-Bromo-3-methyl-2,3-dihydro-1,3-benzoxazol-2-one | [CAS]
67927-44-0 | [Synonyms]
6-bromo-3-methyl-1,3-benzoxazol-2-one 2(3H)-Benzoxazolone, 6-bromo-3-methyl- 6-Bromo-3-methylbenzo[d]oxazol-2(3H)-one 6-Bromo-3-methyl-1,3-benzoxazol-2(3H)-one, 97% 6-Bromo-3-methyl-2,3-dihydro-1,3-benzoxazol-2-one | [Molecular Formula]
C8H6BrNO2 | [MDL Number]
MFCD00694789 | [MOL File]
67927-44-0.mol | [Molecular Weight]
228.04 |
Chemical Properties | Back Directory | [Melting point ]
143-144 °C(Solv: hexane (110-54-3)) | [Boiling point ]
298.2±42.0 °C(Predicted) | [density ]
1.710±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
Powder | [pka]
-1.30±0.20(Predicted) | [color ]
Off-white |
Hazard Information | Back Directory | [Synthesis]
Example 3: Scheme B2; To a solution of 6-bromobenzo[d]oxazol-2(3H)-one (1 eq., 23 mmol, 5.0 g) in acetone (230 ml) was sequentially added potassium carbonate (1.5 eq., 35 mmol, 5.0 g) and iodomethane (1.2 eq., 28 mmol, 4.0 g); The reaction mixture was stirred for 4 hours at room temperature. After completion of the reaction, the acetone solvent was partially concentrated under reduced pressure; the concentrated mixture was poured into 1N HCl aqueous solution and the precipitate was collected by filtration and washed sequentially with water, isopropanol and isopropyl ether to afford 6-bromo-3-methylbenzo[d]oxazol-2(3H)-one (4.22 g, Yield = 79%, Purity (LC) = 99%) as a pinkish pink powder. | [References]
[1] Patent: WO2008/37784, 2008, A1. Location in patent: Page/Page column 35-36 [2] Patent: US2016/289238, 2016, A1. Location in patent: Paragraph 0322; 0323 |
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