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Chloromalonaldehyde → HCID 46785475、化合物

HRID 1257332
ノート
印刷プレビュー

反応式

HRID 1257332 の反応式
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:4]=[C:5]([C:9](=[S:11])[NH2:10])[CH:6]=[CH:7][CH:8]=1.Cl[CH:15]([CH:18]=O)[CH:16]=[O:17]>C(O)C>[F:13][C:2]([F:12])([F:1])[C:3]1[CH:4]=[C:5]([C:9]2[S:11][C:15]([CH:16]=[O:17])=[CH:18][N:10]=2)[CH:6]=[CH:7][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 147646ChloromalonaldehydeHCID 27778493-(Trifluoromethyl)thiobenzamide

生成物 1

HCID 46785475HCID 46785475、化合物収率 25.8%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of 3-(trifluoromethyl)benzenecarbothioamide (1.31 g, 6.37 mmol) in ethanol (15 mL) was added 2-chloropropane-1,3-dial (2.04 g, 19.1 mmol), and the mixture was heated under reflux overnight. The reaction mixture was extracted with ethyl acetate, washed successively with diluted aqueous sodium hydrogen carbonate solution and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (carrier: silica gel, eluent: hexane-ethyl acetate) to give 2-[3-(trifluoromethyl)phenyl]-1,3-thiazole-5-carbaldehyde (423 mg) as colorless crystals. The present compound was dissolved in ethanol (5 mL), sodium borohydride (91 mg, 2.47 mmol) was added under ice-cooling, and the mixture was stirred at room temperature overnight. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate, washed with saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (carrier: silica gel, eluent: hexane-ethyl acetate) to give the title compound (334 mg, 78%) as a colorless oil.

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux overnight
  3. extractionThe reaction mixture was extracted with ethyl acetate
  4. washwashed successively with diluted aqueous sodium hydrogen carbonate solution and saturated brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by column chromatography (carrier: silica gel, eluent: hexane-ethyl acetate)

出典と根拠

ORDレコード
ord-26f4d5995d3445e0aa39835722c95cb5
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08461348B2

反応ノート

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