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2-Bromophenol → 3-(2-Bromophenoxy)-1-isopropylpyrrolidine

HRID 1245858
ノート
印刷プレビュー

反応式

HRID 1245858 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].[H-].[Na+].CS(O[CH:16]1[CH2:20][CH2:19][N:18]([CH:21]([CH3:23])[CH3:22])[CH2:17]1)(=O)=O>CC(N(C)C)=O>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH:16]1[CH2:20][CH2:19][N:18]([CH:21]([CH3:23])[CH3:22])[CH2:17]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 72442-BromophenolHCID 24758Sodium hydrideHCID 219143101-Isopropylpyrrolidin-3-yl methanesulphonate

生成物 1

HCID 219142903-(2-Bromophenoxy)-1-isopropylpyrrolidine

試薬・触媒・溶媒 1

HCID 31374Dimethylacetamide溶媒2 回

反応条件

温度
150 °C

実験手順

To a solution of 2-bromophenol (2.6 g) in dimethylacetamide (20 ml) was added sodium hydride (640 mg) portionwise. A solution of 1-isopropylpyrrolidin-3-yl methanesulphonate [Example 134 (c)] in dimethylacetamide (20 ml) was added and the mixture was heated to 150° C. for 18 h. The mixture was allowed to cool and partitioned between water and dichloromethane. The organic phase was extracted with 2N aqueous hydrochloric acid which was then neutralised and extracted with dichloromethane. The extracts were dried (MgSO4), the solvent removed under vacuum and the product purified by silica chromatography using dichloromethane/aqueous ammonia/methanol mixtures to yield the title compound as a brown oil (496 mg).

後処理

  1. temperatureto cool
  2. custompartitioned between water and dichloromethane
  3. extractionThe organic phase was extracted with 2N aqueous hydrochloric acid which
  4. extractionextracted with dichloromethane
  5. dry with materialThe extracts were dried (MgSO4)
  6. customthe solvent removed under vacuum
  7. customthe product purified by silica chromatography

出典と根拠

ORDレコード
ord-7c5dea4ce75d401f9f11baa818f67ab6
出典データセット
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07125896B2

反応ノート

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