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tert-Butyl 4-chloro-3-oxobutyrate → HCID 178451313、化合物

HRID 1032850
ノート
印刷プレビュー

反応式

HRID 1032850 の反応式
[N:1]([O-:3])=O.[Na+].[Cl:5][CH2:6][C:7](=[O:16])[CH2:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10]>O.C(O)(=O)C.C(=O)(O)[O-].[Na+].[Cl-].[Na+].O>[Cl:5][CH2:6][C:7](=[O:16])/[C:8](=[N:1]/[OH:3])/[C:9]([O:11][C:12]([CH3:14])([CH3:13])[CH3:15])=[O:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 2

HCID 2724514tert-Butyl 4-chloro-3-oxobutyrateHCID 23668193Sodium Nitrite

生成物 1

HCID 178451313HCID 178451313、化合物収率 91%

試薬・触媒・溶媒 4

HCID 176Acetic Acid溶媒HCID 962Water溶媒4 回HCID 516892Sodium Bicarbonate溶媒
HCID 57417360
Sodium chloride; water
溶媒

実験手順

A solution of 35.6 g of sodium nitrite in 100 ml of water was added to a cold solution of t-butyl 4-chloro-3-oxobutanoate (100.9 g, 0.439 moles of 84% material*) in 400 ml of acetic acid containing 50 ml of water over a 0.5 hour period with stirring. The mixture was stirred in the cold for an additional hour, then stored in the cold overnight. The mixture was diluted with 500 ml portions of water, 500 ml of saturated sodium bicarbonate, 500 ml of water and 500 ml of brine, then dried over magnesium sulfate and evaporated to give an amber oil; yield 88.6 g (91% yield). This material was used in the next step without further purification. *This compound was obtained from Lonza Chemical Co., Fair Lawn, N.J.

後処理

  1. stirringThe mixture was stirred in the cold for an additional hour
  2. customstored in the cold overnight
  3. dry with materialdried over magnesium sulfate
  4. customevaporated
  5. customto give an amber oil
  6. customThis material was used in the next step without further purification

出典と根拠

ORDレコード
ord-4742012821f842acac365f48f73492d1
出典データセット
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04959495

反応ノート

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