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Ethyl vinyl ether → 3-(Trifluoromethyl)pyrazole

HRID 875177
ノート
印刷プレビュー

反応式

HRID 875177 の反応式
Cl.[NH2:2][NH2:3].CCO/[CH:7]=[CH:8]/[C:9]([C:11]([F:14])([F:13])[F:12])=O.FC(F)(F)C(Cl)=O.C(OCC)=C>CO>[F:12][C:11]([F:14])([F:13])[C:9]1[CH:8]=[CH:7][NH:3][N:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8023Ethyl vinyl etherHCID 61106Trifluoroacetyl chlorideHCID 115031Hydrazinium chlorideHCID 5709222(3E)-4-Ethoxy-1,1,1-trifluoro-3-buten-2-one

生成物 1

HCID 18070343-(Trifluoromethyl)pyrazole

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 4.4 moles hydrazine.hydrochloride in 2.2 L of methanol in a 3-necked flask, equipped with a mechanical stirrer, a reflux condenser and a dropping funnel an equimolar amount of ETFBO which had been manufactured by addition of trifluoroacetyl chloride to ethyl vinyl ether was added dropwise over about 4 hours under N2 atmosphere. The temperature of the reaction mixture was kept below 15° C. After 12 h of reflux, the reaction batch was filtered in a 2-L flask and concentrated under vacuum (an identical batch was made under the same conditions, yield of both crude products was ca. 95%). Subsequently, the combined crude product was purified by shortpass-vacuum distillation at 27 mbar. The yield was 1105 g, which corresponded to 92% of the theoretical yield.

後処理

  1. additionwas added dropwise over about 4 hours under N2 atmosphere
  2. customwas kept below 15° C
  3. temperatureAfter 12 h of reflux
  4. filtrationthe reaction batch was filtered in a 2-L flask
  5. concentrationconcentrated under vacuum (an identical batch
  6. distillationSubsequently, the combined crude product was purified by shortpass-vacuum distillation at 27 mbar

出典と根拠

ORDレコード
ord-033b39e6ec174a2992d29e1f293ad9b2
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08981115B2

反応ノート

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