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Thionyl Chloride → HCID 15027071、化合物

HRID 2073631
ノート
印刷プレビュー

反応式

HRID 2073631 の反応式
[F:1][C:2]([F:13])([F:12])[CH:3]([CH2:8][CH2:9][CH2:10][CH3:11])[CH2:4][C:5](O)=[O:6].S(Cl)([Cl:16])=O>>[F:1][C:2]([F:13])([F:12])[CH:3]([CH2:8][CH2:9][CH2:10][CH3:11])[CH2:4][C:5]([Cl:16])=[O:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24386Thionyl ChlorideHCID 144070633-Trifluoromethylheptanoic acid

生成物 1

HCID 15027071HCID 15027071、化合物収率 83.1%

実験手順

2.0 g (10 mmol) of 3-trifluoromethylheptanoic acid and 6 ml (about 80 mmol) of thionyl chloride were reacted for 2 hours under heat-refluxing, followed by distillation to obtain 1.8 g of 3-trifluoromethylheptanoic acid chloride (b.p.: 72.2°-75.0° C./25 mmHg). The acid chloride was dissolved in 10 ml of diethyl ether and added dropwise to a preliminarily ice-cooled ether solution of diazomethane, followed by stirring overnight at room temperature. After distilling off the solvent, the remainder was suspended in 15 ml of dioxane and then added to an aqueous solution at 70° C. of 1.1 g of silver oxide and 2.7 g of sodium thiosulfate (penta-hydrate), followed by stirring for 70 min. After the reaction, potassium hydroxide aqueous solution was added thereto and the mixture was filtered. 5N-nitric acid was added to the filtrate to provide an acidity as judged by Congo Red, followed by extraction with diethyl ether. The resultant ether layer was dried with anhydrous sodium sulfate, followed by distilling-off of the solvent and distillation of the product to obtain 0.42 g of objective 4-trifluoromethyloctanoic acid (b.p.: 130°-135° C./26 mmHg).

後処理

  1. temperatureunder heat-refluxing
  2. distillationfollowed by distillation

出典と根拠

ORDレコード
ord-a1efb65882964974a05b8fcab10fc525
出典データセット
uspto-grants-1990_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04918213

反応ノート

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