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Water → 2,1-Benzisothiazole-4-methanol

HRID 1639849
ノート
印刷プレビュー

反応式

HRID 1639849 の反応式
[N:1]1[S:2][CH:3]=[C:4]2[C:9]([C:10](OC)=[O:11])=[CH:8][CH:7]=[CH:6][C:5]=12.[H-].C([Al+]CC(C)C)C(C)C.O>O1CCCC1>[N:1]1[S:2][CH:3]=[C:4]2[C:9]([CH2:10][OH:11])=[CH:8][CH:7]=[CH:6][C:5]=12
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 962WaterHCID 12255806Methyl benzo[c]isothiazole-4-carboxylateHCID 21225700Diisobutylaluminumhydride

生成物 1

HCID 593344662,1-Benzisothiazole-4-methanol収率 98.2%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of methyl 2,1-benzisothiazole-4-carboxylate (5.00 g, 25.9 mmol) in tetrahydrofuran (129 mL) was added diisobutylaluminum hydride (1 M hexane solution, 78.0 mL, 78.0 mmol) at −78° C., and the mixture was stirred at room temperature for 3 hr. The reaction solution was cooled to 0° C., and water was added. The mixture was extracted with ethyl acetate, washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80) to give the title compound (4.2 g, yield 98%).

後処理

  1. temperatureThe reaction solution was cooled to 0° C.
  2. extractionThe mixture was extracted with ethyl acetate
  3. washwashed with saturated brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80)

出典と根拠

ORDレコード
ord-331d46093efd4e009b397c577a85067e
出典データセット
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08110585B2

反応ノート

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