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Triethylamine → (NE)-N-[(7-bromo-2-methyl-1,3-benzoxazol-4-yl)methylidene]hydroxylamine

HRID 536441
ノート
印刷プレビュー

反応式

HRID 536441 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:12]=O)=[C:6]2[C:10]=1[O:9][C:8]([CH3:11])=[N:7]2.Cl.[NH2:15][OH:16].C(N(CC)CC)C>CO.O.C(OCC)(=O)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5](/[CH:12]=[N:15]/[OH:16])=[C:6]2[C:10]=1[O:9][C:8]([CH3:11])=[N:7]2
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 8471TriethylamineHCID 443297Hydroxyamine hydrochlorideHCID 584979577-Bromo-2-methyl-benzo[d]oxazole-4-carbaldehyde

生成物 1

HCID 58498024(NE)-N-[(7-bromo-2-methyl-1,3-benzoxazol-4-yl)methylidene]hydroxylamine収率 105.2%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 962
Water
溶媒
2 回
HCID 8857Ethyl Acetate溶媒

実験手順

To a suspension of 7-bromo-2-methyl-benzo[d]oxazole-4-carbaldehyde (3.23 g) in a mixture of methanol and water (7:3) (60 ml) were added successively hydroxylamine hydrochloride (1.03 g) and triethylamine (2.06 ml) and the reaction mixture was stirred at ambient temperature for 1 hour. The reaction mixture was diluted with ethyl acetate (200 ml) and water (200 ml). The phases were separated and the aqueous phase was extracted with ethyl acetate (150 ml). The combined organic extracts were washed with brine (200 ml), dried over sodium sulfate and concentrated to give (E)-7-bromo-2-methyl-benzo[d]oxazole-4-carbaldehyde oxime (3.61 g) as a brown solid. 1H-NMR (400 MHz, CDCl3): 9.47 (s, 1H) 7.47 (d, 1H), 7.33 (d, 1H), 2.74 (s, 3H) ppm.

後処理

  1. customThe phases were separated
  2. extractionthe aqueous phase was extracted with ethyl acetate (150 ml)
  3. washThe combined organic extracts were washed with brine (200 ml)
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-eee9d53e6beb4fa4895dfaf0d2eeeee4
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08859592B2

反応ノート

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