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Iodine → Tert-butyl 5-chloro-2,4-difluoro-6-iodonicotinate

HRID 1481777
ノート
印刷プレビュー

反応式

HRID 1481777 の反応式
[Li+].[Cl-].[Cl:3][C:4]1[CH:5]=[N:6][C:7]([F:18])=[C:8]([C:16]=1[F:17])[C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10].[I:19]I>C1COCC1>[Cl:3][C:4]1[C:5]([I:19])=[N:6][C:7]([F:18])=[C:8]([C:16]=1[F:17])[C:9]([O:11][C:12]([CH3:14])([CH3:15])[CH3:13])=[O:10]
参加物反応条件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 807IodineHCID 433294Lithium ChlorideHCID 71281897Tert-butyl 5-chloro-2,4-difluoronicotinate

生成物 1

HCID 89421790Tert-butyl 5-chloro-2,4-difluoro-6-iodonicotinate収率 67%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

Into a solution of TMPMgCl LiCl (1.0 M×2.4 mL, 2.4 mmol) in THF at −45° C. was added dropwise a solution of tert-butyl 5-chloro-2,4-difluoronicotinate (0.4 g, 1.6 mmol) in THF (3.0 mL). The mixture was stirred for 20 min then iodine (0.61 g, 2.4 mmol) was added. After 15 min at −45° C., the temperature was allowed to warm to 0° C. The reaction was quenched with saturated NH4Cl and extracted with ethyl acetate. The organic layers were combined, dried over sodium sulfate and evaporated. The residue was purified by silica chromatography (0-5% ethyl acetate in hexanes) to give tert-butyl 5-chloro-2,4-difluoro-6-iodonicotinate (0.4 g, 67%).

後処理

  1. waitAfter 15 min at −45° C.
  2. customThe reaction was quenched with saturated NH4Cl
  3. extractionextracted with ethyl acetate
  4. dry with materialdried over sodium sulfate
  5. customevaporated
  6. customThe residue was purified by silica chromatography (0-5% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-e72e5152d7ec4c9fb8e8b0eca50611b4
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409905B2

反応ノート

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