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Bromine → (S)-(+)-5-Bromo-2-(2-methylbutyloxy)benzonitrile

HRID 651305
ノート
印刷プレビュー

反応式

HRID 651305 の反応式
[CH3:1][C@@H:2]([CH2:13][CH3:14])[CH2:3][O:4][C:5]1[CH:12]=[CH:11][CH:10]=[CH:9][C:6]=1[C:7]#[N:8].[Br:15]Br>>[Br:15][C:10]1[CH:11]=[CH:12][C:5]([O:4][CH2:3][C@@H:2]([CH3:1])[CH2:13][CH3:14])=[C:6]([CH:9]=1)[C:7]#[N:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24408BromineHCID 53752700(S)-(+)-2-(2-Methylbutyloxy)benzonitrile

生成物 1

HCID 53787839(S)-(+)-5-Bromo-2-(2-methylbutyloxy)benzonitrile

実験手順

A mixture of compound 39 (4.25 g, 0.-22 mol), bromine (12.31 g, 0.077 mol was then added and heating continued for another 24 h. The resultant solution was washed with a saturated solution of sodium thiosulphate and finally with water. The dichloromethane solution was dried (MgSO4) and evaporated in vacuo and the crude oil was purified by column chromatography (10% petrol/dichloromethane) to yield a fawn oil.

後処理

  1. additionwas then added
  2. temperatureheating
  3. washThe resultant solution was washed with a saturated solution of sodium thiosulphate and finally with water
  4. dry with materialThe dichloromethane solution was dried (MgSO4)
  5. customevaporated in vacuo
  6. customthe crude oil was purified by column chromatography (10% petrol/dichloromethane)
  7. customto yield a fawn oil

出典と根拠

ORDレコード
ord-09d244bbfa50466ca11c62a4415342a0
出典データセット
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06278028B1

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート