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Sulfuric Acid → 2-Bromo-4,4-dimethylpentanoic acid

HRID 1720983
ノート
印刷プレビュー

反応式

HRID 1720983 の反応式
N[C@H:2]([CH2:6][C:7]([CH3:10])([CH3:9])[CH3:8])[C:3]([OH:5])=[O:4].S(=O)(=O)(O)O.[Br-:16].[K+].N([O-])=O.[Na+]>O>[Br:16][CH:2]([CH2:6][C:7]([CH3:10])([CH3:9])[CH3:8])[C:3]([OH:5])=[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

6

反応物 4

HCID 1118Sulfuric AcidHCID 253877Potassium BromideHCID 69505084-Methyl-D-leucineHCID 23668193Sodium Nitrite

生成物 1

HCID 189159242-Bromo-4,4-dimethylpentanoic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
0 °C

実験手順

A solution of (R)-2-amino-4,4-dimethylpentanoic acid (950 mg, 6.55 mmol) in 2.5N aqueous sulfuric acid (13 ml, 33 mmol) was cooled to -5° C. and treated with potassium bromide (2.72 g, 22.9 mmol) in one portion. The colorless solution was treated with sodium nitrite (680 mg, 9.86 mmol) portionwise, keeping the temperature between 0° and 3° C. over a period of 25 minutes. The reaction mixture was stirred at 0° C. for one hour and at room temperature for 1.5 hours. The reaction mixture was poured into water (10 ml). The product was extracted with ether (60 ml), washed with water (20 ml) and brine (20 ml), dried (magnesium sulfate), and concentrated in vacuo to give the title product as a colorless liquid.

後処理

  1. customthe temperature between 0° and 3° C.
  2. customof 25 minutes
  3. extractionThe product was extracted with ether (60 ml)
  4. washwashed with water (20 ml) and brine (20 ml)
  5. dry with materialdried (magnesium sulfate)
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-6721c8d229ba43a59a34d2dade673432
出典データセット
uspto-grants-1996_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05508272

反応ノート

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