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Diisobutylaluminum hydride → HCID 39232332, 화합물

HRID 1889714
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HRID 1889714 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:13]([Cl:14])=[CH:12][CH:11]=[C:10]([C:15](N(OC)C)=[O:16])[CH:9]=2)=[CH:4][CH:3]=1.CC(C[AlH]CC(C)C)C>C1COCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:13]([Cl:14])=[CH:12][CH:11]=[C:10]([CH:15]=[O:16])[CH:9]=2)=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14487Diisobutylaluminum hydrideHCID 58531623HCID 58531623, 화합물

생성물 1

HCID 39232332HCID 39232332, 화합물수율 87.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

4′,6-Dichloro-N-methoxy-N-methylbiphenyl-3-carboxamide (1.0 g, 3.2 mmol, 1.0 eq) was dissolved in dry THF and stirred for 10 minutes. The solution was cooled to −78° C. and DIBAL-H (1 M solution, 1.83 g, 12.9 mmol, 4 eq, 13 mL) was slowly added over 15-30 minutes. The reaction mixture was stirred for 1 h at −78° C., quenched with saturated NH4Cl solution at −78° C. and stirred for 30 minutes at ambient temperature. Water and ethyl acetate were added into the reaction mixture. The aqueous layer was separated and extracted twice with ethyl acetate. The organic layer was dried with anhydrous Na2SO4 and concentrated under vacuum to give the desired product (0.7 g, 87%). 1H NMR (400 MHz, CDCl3) δ 7.06-7.09 (d, 2H), 7.24-7.27 (d, 2H), 7.40 (s, 1H), 7.55-7.58 (d, 1H), 7.90-7.95 (m, 1H).

후처리

  1. stirringThe reaction mixture was stirred for 1 h at −78° C.
  2. customquenched with saturated NH4Cl solution at −78° C.
  3. stirringstirred for 30 minutes at ambient temperature
  4. additionWater and ethyl acetate were added into the reaction mixture
  5. customThe aqueous layer was separated
  6. extractionextracted twice with ethyl acetate
  7. dry with materialThe organic layer was dried with anhydrous Na2SO4
  8. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-2f5ba791826e4ac0b37ff84529f555f9
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501992B2

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