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tert-Butyl 4-chloro-3-oxobutyrate → HCID 178451313, 화합물

HRID 1032850
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HRID 1032850 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 2

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

생성물 1

HCID 178451313HCID 178451313, 화합물수율 91%

시약·촉매·용매 4

HCID 176Acetic Acid용매HCID 962Water용매4회HCID 516892Sodium Bicarbonate용매
HCID 57417360
Sodium chloride; water
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-4742012821f842acac365f48f73492d1
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04959495

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