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Diethyl Ether → HCID 71743245、化合物

HRID 1423067
ノート
印刷プレビュー

反応式

HRID 1423067 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([CH2:8][C:9]#[N:10])[CH:5]=[CH:4][N:3]=1.Br[CH2:12][CH2:13]Br.CCOCC.[H-].[Na+]>CS(C)=O.CCOC(C)=O.O>[Br:1][C:2]1[CH:7]=[C:6]([C:8]2([C:9]#[N:10])[CH2:13][CH2:12]2)[CH:5]=[CH:4][N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 3283Diethyl EtherHCID 78391,2-DibromoethaneHCID 24758Sodium hydrideHCID 534290262-(2-Bromopyridin-4-YL)acetonitrile

生成物 1

HCID 71743245HCID 71743245、化合物

試薬・触媒・溶媒 3

HCID 679Dimethyl Sulfoxide溶媒2 回
HCID 962
Water
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

A solution of (2-bromopyridin-4-yl)-acetonitrile (1.20 g, 6.09 mmol) and the 1,2-dibromoethane (0.663 mL, 7.61 mmol) in a mixture of anhydrous Et2O (5 mL) and anhydrous DMSO (1 mL) is added to a suspension of NaH (60% dispersion in mineral oil, 585 mg, 14.6 mmol) in anhydrous DMSO (10 mL) while controlling the resulting exotherm by cooling in a water bath, and the resulting mixture is stirred at room temperature. After 18 hours, water (10 mL) and EtOAc (10 mL) are added, phases are separated and the aqueous layer is extracted with EtOAc (3×10 mL). The combined organic layers are washed with brine (30 mL) and dried over MgSO4, filtered and concentrated. The residue is purified by silica gel chromatography eluting with a gradient of 0-60% EtOAc in heptane to afford 1-(2-bromopyridin-4-yl)-cyclopropanecarbonitrile as a solid. MS m/z 223.4, 225.4.

後処理

  1. temperatureby cooling in a water bath
  2. customphases are separated
  3. extractionthe aqueous layer is extracted with EtOAc (3×10 mL)
  4. washThe combined organic layers are washed with brine (30 mL)
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue is purified by silica gel chromatography
  9. washeluting with a gradient of 0-60% EtOAc in heptane

出典と根拠

ORDレコード
ord-20a1c9eb12dd4aa78a9a2c52053a0dd3
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08927550B2

反応ノート

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