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3,4-Dibromothiophene → 3-Bromo-4-(1-oxopropyl)thiophene

HRID 235102
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HRID 235102 반응식
Br[C:2]1[C:6]([Br:7])=[CH:5][S:4][CH:3]=1.C([Li])CCC.CN(OC)[C:15](=[O:18])[CH2:16][CH3:17]>CCOCC>[Br:7][C:6]1[C:2]([C:15](=[O:18])[CH2:16][CH3:17])=[CH:3][S:4][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 184523,4-DibromothiopheneHCID 11344007N-Methoxy-N-methylpropionamideHCID 178418339Butyllithium

생성물 1

HCID 105368333-Bromo-4-(1-oxopropyl)thiophene수율 38.3%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A solution of 3,4-dibromothiophene (6.0 g, 24.8 mmol) in 10 mL of ether was cooled to -78° C. and trated with n-butyllithium (9.92 mL, 2.5M solution in hexanes, 24.8 mmol). While holding the temperature at -78° C., the reaction was stirred for 15 minutes, then 2.9 g (24.8 mmol) of N-methyl-N-methoxypropionamide was added and the reaction was stirred for 1 hour. The reaction was quenched with satd NH4Cl, and the mixture was diluted with ether. The ether layer was separated, washed with water and brine, dried over MgSO4 and concentrated. The residue was triturated with hexanes, and the mixture was filtered. The solvent was removed to give 2.08 g of a tan solid. MS 236, 238 (M+NH4)+. NMR (CDCl3) δ:7.99 (d, J=3 Hz, 1H), 7.32 (d, J=3 Hz, 1H), 2.98 (q, J=7 Hz, 2H), 1.21 (t, J=7 Hz, 3H).

후처리

  1. customat -78° C.
  2. stirringthe reaction was stirred for 1 hour
  3. customThe reaction was quenched with satd NH4Cl
  4. additionthe mixture was diluted with ether
  5. customThe ether layer was separated
  6. washwashed with water and brine
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated
  9. customThe residue was triturated with hexanes
  10. filtrationthe mixture was filtered
  11. customThe solvent was removed

출처 및 근거

ORD 기록
ord-a348106b0b6d43e3a45bb6ec8506f1c4
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05597832

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