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Sodium Bromide → Ethyl 2-bromo-1,3-thiazole-4-carboxylate

HRID 460205
ノート
印刷プレビュー

反応式

HRID 460205 の反応式
[BrH:1].[CH2:2]([O:4][C:5]([C:7]1[N:8]=[C:9](N)[S:10][CH:11]=1)=[O:6])[CH3:3].[Na+].[Br-].N([O-])=O.[Na+]>O.[O-]S([O-])(=O)=O.[Cu+2]>[CH2:2]([O:4][C:5]([C:7]1[N:8]=[C:9]([Br:1])[S:10][CH:11]=1)=[O:6])[CH3:3]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 253881Sodium BromideHCID 16495520Ethyl 2-aminothiazole-4-carboxylate hydrobromideHCID 23668193Sodium Nitrite

生成物 1

HCID 353965Ethyl 2-bromo-1,3-thiazole-4-carboxylate

試薬・触媒・溶媒 2

HCID 24462Copper Sulfate触媒HCID 962Water溶媒2 回

反応条件

温度
0 °C

実験手順

To a stirred mixture of 2-amino-thiazole-4-carboxylic acid ethyl ester hydrobromide (10 g, 58 mmol), CuSO4 (26.9 g, 168 mmol) and NaBr (22.7 g, 221 mmol) in 9M H4SO4 (aq) (120 mL) at −5° C.−0° C., a pre-cooled solution of NaNO2 (4.4 g, 64 mmol) in H2O (40 mL) was added at such a rate to maintain the temperature at or below 0° C. After complete addition the mixture was maintained at 0° C. for another 30 min then warmed to RT over 2.5 h. The reaction mixture was diluted with H2O (120 mL) and extracted with Et2O (3×100 mL). The aqueous layer was separated, basified to pH 12 with 5N NaOH (aq), then extracted with Et2O (2×100 mL). The organic layers were combined, dried over Na2SO4, filtered and the solvent evaporated in vacuo. The residue was purified by flash chromatography on silica gel (1:9, EtOAc:hexane) to yield the title compound as a white amorphous solid. MS m/z: 235.8, 237.8 (M+H). Calc'd. for C6H6BrNO2S-234.93.

後処理

  1. temperatureto maintain the temperature at or below 0° C
  2. additionAfter complete addition the mixture
  3. temperaturethen warmed to RT over 2.5 h
  4. extractionextracted with Et2O (3×100 mL)
  5. customThe aqueous layer was separated
  6. extractionextracted with Et2O (2×100 mL)
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. customthe solvent evaporated in vacuo
  10. customThe residue was purified by flash chromatography on silica gel (1:9, EtOAc:hexane)

出典と根拠

ORDレコード
ord-09c48977aaf044cca773bc8a244988ce
出典データセット
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07196104B2

反応ノート

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