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

HRID 1258802
ノート
印刷プレビュー

反応式

HRID 1258802 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

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.

後処理

  1. temperaturethe reaction mixture was refluxed for 4 h
  2. customAfter complete conversion, reaction mixture
  3. customwas quenched
  4. additionby adding MeOH (10 mL)
  5. customevaporated the solvents
  6. customThe residue obtained
  7. extractionwas extracted with ethyl acetate (30×2 mL)
  8. washthe organic layer was washed with water (20 mL), brine (20 mL) and evaporation of solvent

出典と根拠

ORDレコード
ord-8423cddd08d942849512dd5fb29d074b
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08466114B2

反応ノート

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