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Sulfuric Acid → Tert-butyl 2-bromo-4-methylpentanoate

HRID 636755
ノート
印刷プレビュー

反応式

HRID 636755 の反応式
[Br:1][CH:2]([CH2:6][CH:7]([CH3:9])[CH3:8])[C:3]([OH:5])=[O:4].S(=O)(=O)(O)O.[CH2:15]=[C:16]([CH3:18])[CH3:17]>ClCCl>[Br:1][CH:2]([CH2:6][CH:7]([CH3:9])[CH3:8])[C:3]([O:5][C:16]([CH3:18])([CH3:17])[CH3:15])=[O:4]
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 1118Sulfuric AcidHCID 8255IsobutyleneHCID 1426812-Bromo-4-methylpentanoic acid

生成物 1

HCID 11276775Tert-butyl 2-bromo-4-methylpentanoate収率 98%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-40 °C

実験手順

The product from Step 1 above (63.3 g, 0.32 mol) was dissolved in dichloromethane (250 mL), concentrated sulfuric acid (2 mL) was added, and cooled to −40° C. in a pressure bottle. Isobutene was condensed into the solution to roughly double the volume, and the mixture was then allowed to warm to room temperature overnight. Following evaporation to half of the volume under reduced pressure, the solution was washed with 10% aqueous sodium bicarbonate, dried over Na2SO4, and thoroughly evaporated under reduced pressure at room temperature to leave the title compound as a yellow oil (79.9 g, 0.314 mol; 98%).

後処理

  1. customcondensed into the solution
  2. temperatureto warm to room temperature overnight
  3. customevaporation to half of the volume under reduced pressure
  4. washthe solution was washed with 10% aqueous sodium bicarbonate
  5. dry with materialdried over Na2SO4
  6. customthoroughly evaporated under reduced pressure at room temperature

出典と根拠

ORDレコード
ord-315b50be6d1e4a19b8525ca5a9ac861c
出典データセット
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06194451B1

反応ノート

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