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1-Bromo-3-methylbutan-2-one → HCID 57666787, 화합물

HRID 1445412
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HRID 1445412 반응식
[N+:1]([C:4]1[CH:12]=[C:11]([C:13]([F:16])([F:15])[F:14])[CH:10]=[CH:9][C:5]=1[C:6]([NH2:8])=[S:7])([O-:3])=[O:2].Br[CH2:18][C:19](=O)[CH:20]([CH3:22])[CH3:21]>O1CCOCC1>[CH:20]([C:19]1[N:8]=[C:6]([C:5]2[CH:9]=[CH:10][C:11]([C:13]([F:16])([F:14])[F:15])=[CH:12][C:4]=2[N+:1]([O-:3])=[O:2])[S:7][CH:18]=1)([CH3:22])[CH3:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 108990371-Bromo-3-methylbutan-2-oneHCID 576668062-Nitro-4-(trifluoromethyl)benzenecarbothioamide

생성물 1

HCID 57666787HCID 57666787, 화합물수율 94.8%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

반응 조건

온도
100 °C

실험 절차

2-Nitro-4-trifluoromethyl-thiobenzamide (55), (100 mg, 0.4 mmol) was dissolved in dioxan (4 ml) in a 10 ml test tube and to this solution was added 1-bromo-3-methyl-butan-2-one (52) (72.6 mg, 0.44 mmol). A stirrbar was added and the tube was sealed and heated to 100° C. over night. After cooling to ambient temperature, the vessel was de-capped, the solvent removed in vacuo and the residue partitioned between DCM and 10% aqueous NaHCO3 solution. The organic phase was separated and washed with additional 10% aqueous NaHCO3 solution and brine. The organic phase was filtered through a hydrophobic frit and the solvent removed in vacuo which gave the target compound (120 mg, 90%). LC/MS: (Method I): tR=2.26 min, >90%, m/z (ESI)=317 (MH+).

후처리

  1. additionA stirrbar was added
  2. customthe tube was sealed
  3. temperatureAfter cooling to ambient temperature
  4. customthe solvent removed in vacuo
  5. customthe residue partitioned between DCM and 10% aqueous NaHCO3 solution
  6. customThe organic phase was separated
  7. washwashed with additional 10% aqueous NaHCO3 solution and brine
  8. filtrationThe organic phase was filtered through a hydrophobic frit
  9. customthe solvent removed in vacuo which

출처 및 근거

ORD 기록
ord-dcd1f01dd6d5473ba3c9df6331e6959e
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07666834B2

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