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

HRID 2175179
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HRID 2175179 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 516892Sodium BicarbonateHCID 21226445Aluminium lithium hydrideHCID 584974334,6-Dimethyl-benzo[d]isothiazole-3-carboxylic acid methyl ester

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-ce99b2d8efa3433e97c3397acf4e1d3c
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062056B2

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