Sodium Bicarbonate → Ethyl 2-chloro4-fluoro-5-hydrazinobenzoate

HRID 48484

反応式

HRID 48484 の反応式
C([O-])(=O)C.[Na+].BrC(Br)C(C(F)(F)F)=O.Cl.[Cl:16][C:17]1[CH:27]=[C:26]([F:28])[C:25]([NH:29][NH2:30])=[CH:24][C:18]=1[C:19]([O:21][CH2:22][CH3:23])=[O:20].C(=O)([O-])O.[Na+]>O.C(OCC)C>[Cl:16][C:17]1[CH:27]=[C:26]([F:28])[C:25]([NH:29][NH2:30])=[CH:24][C:18]=1[C:19]([O:21][CH2:22][CH3:23])=[O:20]

参加物

7

実験手順

To a mixed aqueous solution of 5.3 g (53.5 mmol) of sodium acetate and about 100 ml of water was added under ice cooling 6.6 g (24.3 mmol) of 1,1-dibromo-3,3,3-trifluoroacetone, and the reaction was allowed to proceed at 70° C. for 20 minutes. Then, the reaction mixture was cooled to room temperature. Separately, 5.8 g (21.5 mmol) of crude ethyl 2-chloro-4-fluoro-5-hydrazinobenzoate hydrochloride was dissolved in 30 ml of water, to which 100 ml of diethyl ether was added, and while cooling, the mixture was neutralized by the addition of saturated sodium hydrogencarbonate solution, followed by washing with saturated sodium chloride solution, which afforded a solution of ethyl 2-chloro-4-fluoro-5-hydrazinobenzoate in diethyl ether. This solution was added to the above reaction mixture, followed by vigorous stirring at room temperature for 2 hours. The ether layer was separated, washed once with 10 ml of saturated sodium chloride solution, and dried with magnesium sulfate. The diethyl ether was distilled out. The residue was dissolved in 50 ml of THF, to which 8.3 g (23.0 mmol) of carbethoxyethylidenetriphenylphosphorane was added, and the mixture was heated under reflux for 2 hours. The THF was distilled out under reduced pressure, and the residue was subjected to silica gel column chromatography, which afforded 3.8 g (10.0 mmol) of compound 1-642.

後処理

  1. additionwas added
  2. temperaturewhile cooling
  3. washby washing with saturated sodium chloride solution, which

出典と根拠

ORDレコード
ord-2ce17b7d53e64042b768ea5b97dea9c4
出典データセット
uspto-grants-2004_03
特許番号
US06703503B2

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