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Sodium Methoxide → 5-Methoxy-4-methyl-thiazol-2-ylamine

HRID 1009019
ノート
印刷プレビュー

反応式

HRID 1009019 の反応式
Br[C:2]1[S:6][C:5]([NH2:7])=[N:4][C:3]=1[CH3:8].[CH3:9][O-:10].[Na+].ClCCl.O>CO>[CH3:9][O:10][C:2]1[S:6][C:5]([NH2:7])=[N:4][C:3]=1[CH3:8]
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 10942334Sodium MethoxideHCID 129543735-Bromo-4-methyl-1,3-thiazol-2-amineHCID 21908982Water methylene chloride

生成物 1

HCID 204034755-Methoxy-4-methyl-thiazol-2-ylamine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

5-Bromo-4-methyl-thiazol-2-ylamine (0.5 g, 2.59 mmol) was dissolved in methanol abs. (10 mL). The solution was cooled with an ice-bath, then under stirring was added portionwise sodium methoxide (140 mg, 2.59 mmol) The black reaction mixture was stirred for 30 min. at rt then poured into a mixture of dichloromethane/water. The aqueous layer was extracted with two portions of dichloromethane. The combined, organic extracts were dried over magnesium sulfate, filtered and evaporated under reduced pressure to obtain the crude product which was used without further purification. MS (EI): m/e 144.1.

後処理

  1. temperatureThe solution was cooled with an ice-bath
  2. customThe black reaction mixture
  3. stirringwas stirred for 30 min. at rt
  4. extractionThe aqueous layer was extracted with two portions of dichloromethane
  5. dry with materialorganic extracts were dried over magnesium sulfate
  6. filtrationfiltered
  7. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-2984f642682b4c79923f9d53be92f497
出典データセット
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07973051B2

反応ノート

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