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Potassium Carbonate → 5-Bromo-6-methoxybenzo[d]isoxazol-3-ylamine

HRID 2396726
ノート
印刷プレビュー

反応式

HRID 2396726 の反応式
[NH2:1][C:2]1[C:6]2[CH:7]=[CH:8][C:9]([O:11][CH3:12])=[CH:10][C:5]=2[O:4][N:3]=1.[Br:13]Br.C([O-])([O-])=O.[K+].[K+].[O-]S([O-])=O.[Na+].[Na+]>CO.CC(C)=O.C(Cl)(Cl)Cl>[NH2:1][C:2]1[C:6]2[CH:7]=[C:8]([Br:13])[C:9]([O:11][CH3:12])=[CH:10][C:5]=2[O:4][N: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

7

反応物 4

HCID 11430Potassium CarbonateHCID 24408Bromine2 回HCID 24437Sodium SulfiteHCID 106785796-Methoxy-1,2-benzoxazol-3-amine

生成物 1

HCID 187964575-Bromo-6-methoxybenzo[d]isoxazol-3-ylamine収率 67.7%

試薬・触媒・溶媒 2

HCID 887Methanol
溶媒
2 回
HCID 15930782Chloroform acetone溶媒

実験手順

To a stirred solution of 3-amino-6-methoxy-1,2-benzisoxazole (14 g) in methanol (1 L) was added a solution of bromine (13.6 g) and methanol (200 ml) dropwise at -50° C. under N2. The mixture was allowed to warm to room temperature after the addition was complete. After 24 hours an additional 1/4 equivalent of bromine was added. TLC (10% acetone/CHCl3) showed no starting material 24 hours later. The reaction was neutralized with saturated K2CO3 solution, treated with saturated Na2SO3 solution triturated with water, filtered, and washed with water. The crude product was dried in vacuo affording 14 g of product, m.p. 226°-227° C.

後処理

  1. additionafter the addition
  2. customno starting material 24 hours
  3. customtriturated with water
  4. filtrationfiltered
  5. washwashed with water
  6. dry with materialThe crude product was dried in vacuo

出典と根拠

ORDレコード
ord-c5b55bef8ab349fc9ad59fb32009f32e
出典データセット
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05494908

反応ノート

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