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4-Methoxy-2-aminobenzothiazole → 2-Bromo-4-methoxy-1,3-benzothiazole

HRID 427286
ノート
印刷プレビュー

反応式

HRID 427286 の反応式
N[C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH3:12])[C:5]=2[N:6]=1.[Br-:13].[K+].N([O-])=O.[Na+]>S(=O)(=O)(O)O>[Br:13][C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH3:12])[C:5]=2[N:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 216224-Methoxy-2-aminobenzothiazoleHCID 253877Potassium BromideHCID 23668193Sodium Nitrite

生成物 1

HCID 183569972-Bromo-4-methoxy-1,3-benzothiazole収率 78.8%

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

実験手順

To a solution of 2-amino-4-methoxybenzothiazole (1.5 g) and potassium bromide (3.5 g) in sulphuric acid (1.25M, 50 ml) at 0° C. was added sodium nitrite (0.86 g) over a period of 1 hr. The reaction was allowed to warm to room temperature and stirred for 2 hrs, before being extracted with dichloromethane (3×50 ml). The combined organic extracts were dried over magnesium sulphate (5 g), and the solvent removed in vacuo to yield an off white solid. This was purified by flash chromatography (eluent 50% ethyl acetate/hexane) to yield the title compound as a white solid (1.6 g). TLC Ff 0.30 (20% ethyl acetate in hexane)

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. extractionbefore being extracted with dichloromethane (3×50 ml)
  2. dry with materialThe combined organic extracts were dried over magnesium sulphate (5 g)
  3. customthe solvent removed in vacuo
  4. customto yield an off white solid
  5. customThis was purified by flash chromatography (eluent 50% ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-d1caa672c92a4f6d8821d2f04995a1c3
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06313116B1

反応ノート

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