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Diethyl Ether → 2-Fluoro-4-[1-hydroxy-1-(3-methyl-3H-imidazol-4-yl)-ethyl]-benzonitrile

HRID 379068
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HRID 379068 반응식
[F:1][C:2]1[CH:9]=[C:8]([C:10]([C:12]2[N:13]([CH3:17])[CH:14]=[N:15][CH:16]=2)=[O:11])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].C[Mg+].[Br-].[CH2:21](OCC)C>C1COCC1>[F:1][C:2]1[CH:9]=[C:8]([C:10]([OH:11])([C:12]2[N:13]([CH3:17])[CH:14]=[N:15][CH:16]=2)[CH3:21])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5]
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참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 185332052-Fluoro-4-(3-methyl-3H-imidazole-4-carbonyl)-benzonitrileHCID 178418689HCID 178418689, 화합물

생성물 1

HCID 216969592-Fluoro-4-[1-hydroxy-1-(3-methyl-3H-imidazol-4-yl)-ethyl]-benzonitrile

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

2-Fluoro-4-(3-methyl-3H-imidazole-4-carbonyl)-benzonitrile (0.603 g, 2.63 mmol) was dissolved in anhydrous THF (30 mL). A solution of 3.0M MeMgBr in diethyl ether (2.55 mL, 7.65 mmol) was added and stirred for 15 min. The reaction was quenched with NH4Cl solution, diluted with CH2Cl2 and saturated NaHCO3 solution and seperated. The aqueous layer was back extracted with CH2Cl2 (3×), the combined organic layers dried (MgSO4) and concentrated to give the title compound.

후처리

  1. customThe reaction was quenched with NH4Cl solution
  2. additiondiluted with CH2Cl2 and saturated NaHCO3 solution
  3. customseperated
  4. extractionThe aqueous layer was back extracted with CH2Cl2 (3×)
  5. dry with materialthe combined organic layers dried (MgSO4)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2f279e0800d9483cbacc09df09c2e548
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06297239B1

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