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Dimethylformamide → 3-Bromoquinoline-2-carbaldehyde

HRID 389281
ノート
印刷プレビュー

反応式

HRID 389281 の反応式
CC1(C)CCCC(C)(C)N1.[Br:11][C:12]1[CH:13]=[N:14][C:15]2[C:20]([CH:21]=1)=[CH:19][CH:18]=[CH:17][CH:16]=2.CN([CH:25]=[O:26])C>C1COCC1>[Br:11][C:12]1[C:13]([CH:25]=[O:26])=[N:14][C:15]2[C:20]([CH:21]=1)=[CH:19][CH:18]=[CH:17][CH:16]=2
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6228DimethylformamideHCID 130352,2,6,6-TetramethylpiperidineHCID 214133-Bromoquinoline

生成物 1

HCID 573555563-Bromoquinoline-2-carbaldehyde

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To isopropylmagnesium chloride lithium chloride complex solution (1.3M in THF; 50 mL, 65 mmol) was added 2,2,6,6-tetramethylpiperidine (11.5 mL, 68.3 mmol) dropwise, and the mixture was stirred overnight at room temperature. To 55 mL of the resulting solution at −25° C. under N2 was added 3-bromoquinoline (6.52 mL, 48 mmol) dropwise, and the reaction was stirred for 1 hour. DMF (3 mL) was added, and the reaction was slowly warmed to room temperature and monitored by analytical LCMS. The mixture was quenched with saturated aqueous NH4Cl and worked-up. The residue was purified by silica gel chromatography to give the title compound.

後処理

  1. stirringthe reaction was stirred for 1 hour
  2. temperaturethe reaction was slowly warmed to room temperature
  3. customThe mixture was quenched with saturated aqueous NH4Cl
  4. customThe residue was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-8977e22ea4e84de89bac11b74a0109cb
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08378107B2

反応ノート

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