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Sodium Bicarbonate → (4,6-Dimethyl-1,2-benzisothiazol-3-yl)-methanol

HRID 2175179
ノート
印刷プレビュー

反応式

HRID 2175179 の反応式
C[O:2][C:3]([C:5]1[C:9]2[C:10]([CH3:15])=[CH:11][C:12]([CH3:14])=[CH:13][C:8]=2[S:7][N:6]=1)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O-])(O)=O.[Na+]>C1COCC1>[CH3:15][C:10]1[C:9]2[C:5]([CH2:3][OH:2])=[N:6][S:7][C:8]=2[CH:13]=[C:12]([CH3:14])[CH:11]=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 516892Sodium BicarbonateHCID 21226445Aluminium lithium hydrideHCID 584974334,6-Dimethyl-benzo[d]isothiazole-3-carboxylic acid methyl ester

生成物 1

HCID 58497417(4,6-Dimethyl-1,2-benzisothiazol-3-yl)-methanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 4,6-dimethyl-benzo[d]isothiazole-3-carboxylic acid methyl ester (100 mg, 0.45 mmol) in THF (10 mL) was added lithium aluminum hydride (LiAlH4) (34 mg, 0.9 mmol) at 0° C. under nitrogen atmosphere. The solution was stirred at the same temperature for 1 hour. Sat. NaHCO3 was added and the solution was extracted with EtOAc. The combined organic layer was dried with MgSO4 and filtered. The filtrate was concentrated and the residue was used in the next step of the synthesis without further purification.

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. extractionthe solution was extracted with EtOAc
  2. dry with materialThe combined organic layer was dried with MgSO4
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated
  5. customthe residue was used in the next step of the synthesis without further purification

出典と根拠

ORDレコード
ord-ce99b2d8efa3433e97c3397acf4e1d3c
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09062056B2

反応ノート

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