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p-Fluoronitrobenzene → HCID 68696157、化合物

HRID 2352900
ノート
印刷プレビュー

反応式

HRID 2352900 の反応式
[F:1][CH:2]1[CH2:6][CH2:5][N:4]([CH2:7][CH2:8][CH2:9][OH:10])[CH2:3]1.CC([O-])(C)C.[K+].F[C:18]1[CH:23]=[CH:22][C:21]([N+:24]([O-:26])=[O:25])=[CH:20][CH:19]=1>C1COCC1>[F:1][CH:2]1[CH2:6][CH2:5][N:4]([CH2:7][CH2:8][CH2:9][O:10][C:18]2[CH:23]=[CH:22][C:21]([N+:24]([O-:26])=[O:25])=[CH:20][CH:19]=2)[CH2:3]1
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 9590p-FluoronitrobenzeneHCID 179805453-(3-Fluoropyrrolidin-1-yl)propan-1-olHCID 23665647Potassium tert-butoxide

生成物 1

HCID 68696157HCID 68696157、化合物収率 82%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

The crude 3-(3-Fluoro-pyrrolidin-1-yl)-propan-1-ol (assumed 3.06 mmol) was dissolved in THF (8 mL) and was cooled to 0° C. The 0° C. solution was treated consecutively with KOtBu (1.5 g, 13.5 mmol) then 4-fluoronitrobenzene (423.3 mg, 3 mmol). The resulting reaction mixture was allowed to warm to room temperature and stir for an additional 4.5 h. The reaction mixture was quenched with the addition of ice water (50 mL) followed by extraction with EtOAc (75 mL). The organics were subsequently washed with room temperature H2O (75 mL), then saturated NaHCO3 (aq) (75 mL), and finally with brine (75 mL). The organics then were dried over anhydrous sodium sulfate, decanted and concentrated in vacuo to yield crude 3-Fluoro-1-[3-(4-nitro-phenoxy)-propyl]-pyrrolidine (660 mg) as a yellow oil. This material was carried on without further purification.

後処理

  1. customThe resulting reaction mixture
  2. temperatureto warm to room temperature
  3. customThe reaction mixture was quenched with the addition of ice water (50 mL)
  4. extractionfollowed by extraction with EtOAc (75 mL)
  5. washThe organics were subsequently washed with room temperature H2O (75 mL)
  6. dry with materialThe organics then were dried over anhydrous sodium sulfate
  7. customdecanted
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-311856f481414d098697137369f2e7da
出典データセット
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07749530B2

反応ノート

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