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Sulfuryl chloride → HCID 18630151, 화합물

HRID 534831
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HRID 534831 반응식
[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[NH:11][C:12](=[O:14])[CH3:13])([CH3:4])([CH3:3])[CH3:2].S(Cl)([Cl:18])(=O)=O>C(O)(=O)C>[C:1]([C:5]1[CH:10]=[C:9]([Cl:18])[CH:8]=[CH:7][C:6]=1[NH:11][C:12](=[O:14])[CH3:13])([CH3:4])([CH3:2])[CH3:3]
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참가 물질

4

반응물 2

HCID 24648Sulfuryl chlorideHCID 343805N-(2-tert-butylphenyl)acetamide

생성물 1

HCID 18630151HCID 18630151, 화합물수율 53.3%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
50 °C

실험 절차

A mixture of N-(2-tert-butylphenyl)acetamide (Reference Example 17, 5.93 g, 31.0 mmol) and sulfuryl chloride (10.5 g, 77.5 mmol) in acetic acid (190 mL) was stirred at 50° C. for 16 h. The reaction mixture was partitioned between ethyl acetate and water, and the organic layer was washed with 10% aqueous NaHCO3, and saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting solid was recrystallized from toluene/diethyl ether to give the title compound (3.73 g) as a white solid. The mother liquid was concentrated under reduced pressure and the residue was purified by flash column chromatography (silica gel, 4:1-1:4 hexane/ethyl acetate) to provide the title compound (1.05 g) as a white solid.

후처리

  1. customThe reaction mixture was partitioned between ethyl acetate and water
  2. washthe organic layer was washed with 10% aqueous NaHCO3, and saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe resulting solid was recrystallized from toluene/diethyl ether

출처 및 근거

ORD 기록
ord-7775d21209f441daba1dfce70ef1324b
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08853215B2

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