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Water → HCID 22494742, 화합물

HRID 1816705
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HRID 1816705 반응식
CS(O[CH:6]1[CH2:11][CH2:10][N:9]([C:12]2[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[CH:14][CH:13]=2)[CH2:8][CH2:7]1)(=O)=O.[C:21]([O-:24])(=[S:23])[CH3:22].[K+].O>CS(C)=O>[C:21]([S:23][CH:6]1[CH2:7][CH2:8][N:9]([C:12]2[CH:13]=[CH:14][C:15]([N+:18]([O-:20])=[O:19])=[CH:16][CH:17]=2)[CH2:10][CH2:11]1)(=[O:24])[CH3:22]
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참가 물질

5

반응물 3

HCID 962WaterHCID 22494745HCID 22494745, 화합물HCID 23670855Potassium ethanethioate

생성물 1

HCID 22494742HCID 22494742, 화합물수율 61.6%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

A solution of 4-[4-(methanesulfonyloxy)piperidin-1-yl]nitrobenzene (2.0 g), and potassium thioacetate (1.14 g) in dimethylsulfoxide (DMSO) (20 ml) was stirred at 100-110° C. for 3 hours. The reaction mixture was poured into water (100 ml) and extracted twice with ethyl acetate (100 ml). The extracts were collected, washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo. The resulting precipitates were washed with IPE (50 ml), collected by filtration and dried in vacuo to give 4-(4-acetylthiopiperidin-1-yl)nitrobenzene (1.15 g).

후처리

  1. extractionextracted twice with ethyl acetate (100 ml)
  2. customThe extracts were collected
  3. washwashed with saturated aqueous sodium chloride
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customevaporated in vacuo
  6. customThe resulting precipitates
  7. washwere washed with IPE (50 ml)
  8. filtrationcollected by filtration
  9. customdried in vacuo

출처 및 근거

ORD 기록
ord-d498a9bf76d6455d91d93ababd0d176a
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06884868B1

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