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Hydrochloric Acid → HCID 10943963, 화합물

HRID 387344
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HRID 387344 반응식
[Br:1][C:2]1[CH:3]=[C:4]([C:7](=O)[CH:8]([CH3:10])[CH3:9])[S:5][CH:6]=1.O.NN.Cl>C(O)CO.O>[Br:1][C:2]1[CH:3]=[C:4]([CH2:7][CH:8]([CH3:10])[CH3:9])[S:5][CH:6]=1
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 24654Hydrazine hydrate (1:1)HCID 593327031-(4-Bromothiophen-2-yl)-2-methylpropan-1-one

생성물 1

HCID 10943963HCID 10943963, 화합물수율 25%

시약·촉매·용매 2

HCID 174Ethylene Glycol용매HCID 962Water용매

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온도
160 °C

실험 절차

1-(4-bromo-2-thienyl)-2-methyl-1-propanone (816 mg, 3.52 mmol) was diluted in ethylene glycol (3 mL). Hydrazine monohydrate (0.46 mL, 9.5 mmol, 2.7 eq) was added, and the mixture was heated to 160° C. for 1.5 h behind a blast shield. The mixture was cooled to rt, and diluted with water. 6 M aqueous HCl was added until pH was acidic (pH paper), and the mixture was extracted three times with hexanes. The combined organics were dried over sodium sulfate, filtered, and concentrated. The crude product was purified by biotage, 25M+ column, eluting with 5% ethyl acetate in hexanes. Fractions containing the desired product were concentrated in vacuo to afford the title compound as light yellow oil (192 mg, 25%).

후처리

  1. temperatureThe mixture was cooled to rt
  2. extractionthe mixture was extracted three times with hexanes
  3. dry with materialThe combined organics were dried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude product was purified by biotage, 25M+ column
  7. washeluting with 5% ethyl acetate in hexanes
  8. additionFractions containing the desired product
  9. concentrationwere concentrated in vacuo

출처 및 근거

ORD 기록
ord-fdb044e128574a9f9889e4ed97eefb86
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08372875B2

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