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Diisobutylaluminumhydride → 4,5-Dibromofuran-2-carbaldehyde

HRID 271513
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HRID 271513 반응식
[H-].C([Al+]CC(C)C)C(C)C.CON(C)[C:14]([C:16]1[O:17][C:18]([Br:22])=[C:19]([Br:21])[CH:20]=1)=[O:15]>O1CCCC1>[Br:21][C:19]1[CH:20]=[C:16]([CH:14]=[O:15])[O:17][C:18]=1[Br:22]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21225700DiisobutylaluminumhydrideHCID 446297544,5-Dibromo-N-methoxy-N-methylfuran-2-carboxamide

생성물 1

HCID 10852284,5-Dibromofuran-2-carbaldehyde수율 81%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
-78 °C

실험 절차

Diisobutylaluminum hydride (80 ml, 1M solution in toluene) was added to a solution of the product from Step 2 (20 g, 63.4 mmol) in tetrahydrofuran (160 ml) at −78° C. The mixture was stirred at −78° C. for 1.5 hours and was then quenched with a saturated aqueous solution of ammonium chloride (40 ml). The reaction was allowed to warm to room temperature, diluted with ethyl acetate and 5M hydrochloric acid (20 ml) and stirred for 30 minutes. The organic layer was separated, washed twice with water and then brine, dried and concentrated in vacuo to yield the title compound (12.9 g, 81%); 1H NMR (CDCl3) 9.52 (1H, s), 7.21 (1H, s).

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후처리

  1. customwas then quenched with a saturated aqueous solution of ammonium chloride (40 ml)
  2. temperatureto warm to room temperature
  3. additiondiluted with ethyl acetate and 5M hydrochloric acid (20 ml)
  4. stirringstirred for 30 minutes
  5. customThe organic layer was separated
  6. washwashed twice with water
  7. dry with materialbrine, dried
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-db7036dbb1054244abd4b549c6e7eaf8
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07452906B2

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