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Diisobutylaluminum hydride → (4-(Trifluoromethyl)-1,3-thiazol-2-yl)methanol

HRID 2062124
ノート
印刷プレビュー

反応式

HRID 2062124 の反応式
C([O:3][C:4]([C:6]1[S:7][CH:8]=[C:9]([C:11]([F:14])([F:13])[F:12])[N:10]=1)=O)C.CC(C[AlH]CC(C)C)C>C1COCC1>[F:14][C:11]([F:12])([F:13])[C:9]1[N:10]=[C:6]([CH2:4][OH:3])[S:7][CH:8]=1
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

4

反応物 2

HCID 14487Diisobutylaluminum hydrideHCID 23560697Ethyl 4-(trifluoromethyl)thiazole-2-carboxylate

生成物 1

HCID 23560688(4-(Trifluoromethyl)-1,3-thiazol-2-yl)methanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

4-Trifluoromethyl-thiazole-2-carboxylic acid ethyl ester (131 mg) was dissolved in THF (5 ml). The reaction mixture was then cooled to −78° C. DIBAL-H (4.7 ml, 1.0 M in tetrahydrofurane) was added slowly during a period of 10 min. The cooling bath was removed, and the solution was kept under stirring for 30 min at RT. The solution was then cooled to 0° C., and NaF (784 mg) was added, followed by the slow addition of 3 ml water. The product was extracted by ethyl acetate. The solvent was removed, and the crude product was used in alkylation reactions without further purification.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. customThe cooling bath was removed
  2. temperatureThe solution was then cooled to 0° C.
  3. additionNaF (784 mg) was added
  4. additionfollowed by the slow addition of 3 ml water
  5. extractionThe product was extracted by ethyl acetate
  6. customThe solvent was removed
  7. customthe crude product was used in alkylation reactions without further purification

出典と根拠

ORDレコード
ord-72c93f292b324972a66dfae5f58af0b6
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08283479B2

反応ノート

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