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Pyridine → HCID 71014114, 화합물

HRID 1773811
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HRID 1773811 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:9](O)([C:26]([F:29])([F:28])[F:27])[CH2:10][C:11]([C:13]2[S:17][C:16]([C:18]([O:20][CH3:21])=[O:19])=[C:15]3[CH2:22][CH2:23][CH2:24][CH2:25][C:14]=23)=[O:12])[CH:5]=[C:6]([Cl:8])[CH:7]=1.O=S(Cl)Cl.N1C=CC=CC=1>C(Cl)Cl.[NH4+].[Cl-]>[CH3:21][O:20][C:18]([C:16]1[S:17][C:13]([C:11](=[O:12])[CH:10]=[C:9]([C:4]2[CH:5]=[C:6]([Cl:8])[CH:7]=[C:2]([Cl:1])[CH:3]=2)[C:26]([F:29])([F:28])[F:27])=[C:14]2[CH2:25][CH2:24][CH2:23][CH2:22][C:15]=12)=[O:19]
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참가 물질

6

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HCID 1049PyridineHCID 24386Thionyl ChlorideHCID 71014111Methyl 3-(3-(3,5-dichlorophenyl)-4,4,4-trifluoro-3-hydroxybutanoyl)-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carboxylate

생성물 1

HCID 71014114HCID 71014114, 화합물수율 100%

시약·촉매·용매 2

HCID 6344Dichloromethane용매
HCID 25517
Ammonium Chloride
용매

실험 절차

Stir a mixture of methyl 3-(3-(3,5-dichlorophenyl)-4,4,4-trifluoro-3-hydroxyl butanoyl)-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carboxylate (9.1 g, 18.9 mmol), SOCl2 (9.0 g, 5.5 mL, 75.6 mmol) and pyridine (2.99 g, 3.1 mL, 37.8 mmol) in anhydrous DCM (100 mL) at ambient temperature overnight. Dilute the resultant mixture with saturated NH4Cl aqueous solution. Extract the aqueous mixture with DCM (100 mL×3). The combined organic layers are washed with brine, dried over anhydrous Na2SO4 and concentrated under vacuum. Purify the residue by silica gel chromatograph (PE:EtOAc 50:1) to afford 3-[3-(3,5-Dichloro-phenyl)-4,4,4-trifluoro-but-2-enoyl]-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid methyl ester as an orange solid (8.75 g, 100%). (m/z): 463 (M+1).

후처리

  1. extractionExtract the aqueous mixture with DCM (100 mL×3)
  2. washThe combined organic layers are washed with brine
  3. dry with materialdried over anhydrous Na2SO4
  4. concentrationconcentrated under vacuum
  5. customPurify the residue by silica gel chromatograph (PE:EtOAc 50:1)

출처 및 근거

ORD 기록
ord-bbf5d1b818b84768ac82349cf7020745
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09255111B2

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