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Dimethylformamide → 4-Ethylthiophene-3-carboxaldehyde

HRID 1290242
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인쇄 미리보기

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HRID 1290242 반응식
Br[C:2]1[C:6]([CH2:7][CH3:8])=[CH:5][S:4][CH:3]=1.[Li]CCCC.CN([CH:17]=[O:18])C>C(OCC)C>[CH2:7]([C:6]1[C:2]([CH:17]=[O:18])=[CH:3][S:4][CH:5]=1)[CH3:8]
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참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 1279238983663-39-2HCID 178418339Butyllithium

생성물 1

HCID 189238504-Ethylthiophene-3-carboxaldehyde

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
-20 °C

실험 절차

A solution of 3-bromo-4-ethylthiophene, B9, (3.4 g, 0.018 mol) in 40 mL of diethyl ether was cooled to -78° C., and a solution of n-BuLi (12.0 mL, 1.6M) in hexanes was added dropwise. The solution was allowed to warm to -20° C., and DMF (1.46 g, 0.020 mol) was added. The reaction mixture was allowed to warm to ambient temperature and was stirred overnight. The reaction was quenched with aqueous ammonium chloride solution and extracted twice with diethyl ether. The organic extracts were combined, washed with twice with water and then brine and dried (MgSO4). The solution was filtered and concentrated to provide 4-ethylthiophene-3-carboxaldehyde, C9, which was used directly in the next step. ##STR65##

후처리

  1. temperatureto warm to ambient temperature
  2. customThe reaction was quenched with aqueous ammonium chloride solution
  3. extractionextracted twice with diethyl ether
  4. washwashed with twice with water
  5. dry with materialbrine and dried (MgSO4)
  6. filtrationThe solution was filtered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-01f371808dbf4eadbd6df805f21b0e69
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05750720

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