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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Hydrazine hydrate (1:1) → Styrene

HRID 1284286
ノート
印刷プレビュー

反応式

HRID 1284286 の反応式
[C:1]([O:5][CH3:6])(=[O:4])[CH:2]=[CH2:3].[CH2:7]=[CH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.O.NN>C(O)C>[C:1]([O:5][CH3:6])(=[O:4])[CH:2]=[CH2:3].[CH2:7]=[CH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 22731677Methyl Acrylate Styrene

生成物 2

HCID 7294Methyl Acrylate収率 22%HCID 7501Styrene収率 50%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

In a 500-ml three-necked round-bottomed flask equipped with a magnetic stirrer, condenser, and nitrogen sweep were placed the methyl acrylate-styrene copolymer (50.0 g), ethanol (200 ml), and 85% hydrazine hydrate (100 ml). The reaction mixture was stirred and heated at reflux for 48 hours. The cooled reaction mixture was poured slowly into distilled water (200 ml) being agitated in an air-driven blender. The white precipitate was collected on a Buchner funnel, sucked dry, and vacuum-dried at 50°C. This procedure yields a poly(hydrazide) containing 28% hydrazide, 22% methyl acrylate, and 50% styrene when starting with the 50/50 copolymer. The proportion of hydrazide can be increased by using longer reaction times. The reaction time can be halved by substituting dimethyl sulfoxide for ethanol but the recovery step takes more time.

後処理

  1. customIn a 500-ml three-necked round-bottomed flask equipped with a magnetic stirrer, condenser
  2. temperatureheated
  3. temperatureat reflux for 48 hours
  4. customThe cooled reaction mixture
  5. additionwas poured slowly
  6. distillationinto distilled water (200 ml)
  7. stirringbeing agitated in an air-driven blender
  8. customThe white precipitate was collected on a Buchner funnel
  9. customsucked dry
  10. customvacuum-dried at 50°C

出典と根拠

ORDレコード
ord-a3cef5c8a84c4597906dbd468590e5f8
出典データセット
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03978156

反応ノート

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