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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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Water → HCID 12899414、化合物

HRID 1979759
ノート
印刷プレビュー

反応式

HRID 1979759 の反応式
[C:1]([O:4][C:5]1[CH:14]=[CH:13][CH:12]=[C:11]2[C:6]=1[CH2:7][CH2:8][C:9](=[O:15])[NH:10]2)(=[O:3])[CH3:2].[Br:16]Br.O>C(O)(=O)C>[Br:16][C:12]1[CH:13]=[CH:14][C:5]([O:4][C:1](=[O:3])[CH3:2])=[C:6]2[C:11]=1[NH:10][C:9](=[O:15])[CH2:8][CH2:7]2
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 3

HCID 962WaterHCID 24408BromineHCID 128994132-Oxo-1,2,3,4-tetrahydroquinolin-5-yl acetate

生成物 1

HCID 12899414HCID 12899414、化合物

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

実験手順

20.5 Grams of 5-acetyloxy-3,4-dihydrocarbostyril was dissolved in 200 ml of acetic acid, into this solution, 16 g of bromine dissolved in 60 ml of acetic acid was added dropwise under water-cooled condition with stirring for 30 minutes and the reaction was continued for 2 hours at the same temperature. Then 300 ml of water added to this reaction mixture and allowed to stand for 3 hours, and crystals formed in the mixture were obtained by filtration and recrystallized from methanol. 21 Grams of 8-bromo-5-acetyloxy-3,4-dihydrocarbostyril was obtained as in the form of colorless needle-like crystals. Melting point: 237°-239° C.

後処理

  1. additionwas added dropwise under water-
  2. temperaturecooled condition
  3. waitthe reaction was continued for 2 hours at the same temperature
  4. waitto stand for 3 hours
  5. customcrystals formed in the mixture
  6. customwere obtained by filtration
  7. customrecrystallized from methanol

出典と根拠

ORDレコード
ord-ce8eb4261354470fbdf9a8f71c11f891
出典データセット
uspto-grants-1984_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04482560

反応ノート

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