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Chemical Structure| 1414377-89-1 Chemical Structure| 1414377-89-1

Structure of 1414377-89-1

Chemical Structure| 1414377-89-1

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Product Details of [ 1414377-89-1 ]

CAS No. :1414377-89-1
Formula : C11H12O3S
M.W : 224.28
SMILES Code : O=C(C1=C2C(CCC2)=C(C(C)=O)S1)OC
MDL No. :MFCD28347696

Safety of [ 1414377-89-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1414377-89-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1414377-89-1 ]

[ 1414377-89-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1190865-44-1 ]
  • [ 1414377-89-1 ]
  • [ 1414377-96-0 ]
YieldReaction ConditionsOperation in experiment
89.3% I) Synthesis of3-[3-(3,5-Dichloro-4-fluoro-phenyl)-4,4,4-trifluoro-3-hydroxy-butyryl]-5,6- dihydro-4H-cyclopenta[c]thiophene-l-carboxylic acid methyl esterAdd a solution of LiHDMS (1M in THF, 75 mL, 75 mmol) to a suspension of 3-acetyl-5,6-dihydro-4H-cyclopenta[c]thiophene-l-carboxylic acid methyl ester (14.0 g, 62.5 mmol) in dry THF (200 mL) at -78C under N2. After stirring at room temperature for 1.5 h, add l-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone (17.9 g, 68.7 mmol) in dry THF (100 mL) to the reaction mixture and stir the resultant mixture at the same temperature for additional 2 hours. Quench the reaction with saturated NH4C1 aqueous solution. Extract the aqueous mixture with EtOAc (100 mL><3). The combined organic layers are washed with brine, dried over anhydrous a2S04 and concentrated under vacuum. Purify the residue by silica gel chromatograph (PE:EtOAc 15: 1) to afford 3-[3-(3,5-Dichloro-4-fluoro-phenyl)-4,4,4-trifluoro-3-hydroxy-butyryl]-5,6-dihydro-4H-cyclopenta [c]thiophene-l-carboxylic acid methyl ester as an orange solid (27 g, 89.3%). MS (m/z): 486 (M+l).
89.3% I) Synthesis of3-[3-(3,5-Dichloro-4-fluoro-phenyl)-4,4,4-trifluoro-3-hydroxy-butyryl]-5,6- dihydro-4H-cyclopenta[c]thiophene-l-carboxylic acid methyl esterAdd a solution of LiHDMS (1M in THF, 75 mL, 75 mmol) to a suspension of 3-acetyl-5,6-dihydro-4H-cyclopenta[c]thiophene-l-carboxylic acid methyl ester (14.0 g, 62.5 mmol) in dry THF (200 mL) at -78C under N2. After stirring at room temperature for 1.5 h, add l-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone (17.9 g, 68.7 mmol) in dry THF (100 mL) to the reaction mixture and stir the resultant mixture at the same temperature for additional 2 hours. Quench the reaction with saturated NH4C1 aqueous solution. Extract the aqueous mixture with EtOAc (100 mL><3). The combined organic layers are washed with brine, dried over anhydrous a2S04 and concentrated under vacuum. Purify the residue by silica gel chromatograph (PE:EtOAc 15: 1) to afford 3-[3-(3,5-Dichloro-4-fluoro-phenyl)-4,4,4-trifluoro-3-hydroxy-butyryl]-5,6-dihydro-4H-cyclopenta [c]thiophene-l-carboxylic acid methyl ester as an orange solid (27 g, 89.3%). MS (m/z): 486 (M+l).
 

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