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Hydrochloric Acid → HCID 86654325、化合物

HRID 1404086
ノート
印刷プレビュー

反応式

HRID 1404086 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([N+:9]([O-])=O)=[C:4]([Br:12])[C:3]=1[O:13][CH3:14].Cl.Cl[Sn]Cl.O>C(O)C>[Br:12][C:4]1[C:3]([O:13][CH3:14])=[C:2]([Br:1])[CH:7]=[C:6]([F:8])[C:5]=1[NH2:9]
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 313Hydrochloric AcidHCID 225046691,3-Dibromo-5-fluoro-2-methoxy-4-nitrobenzeneHCID 43835034Tin dichloride dihydrate

生成物 1

HCID 86654325HCID 86654325、化合物収率 100%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To the solution of 8-4 (234.2 g, 0.784 mol) and concentrated HCl (720 mL) in ethanol (2.2 L) at room temperature, SnCl2.H2O (415 g, 2.0 mol) was added by portions. The mixture was stirred for 16 h. TLC showed the reaction was completed. The volatiles were removed in vacuo. The residue was quenched with cooled water (500 mL) and ethyl acetate (1.5 L). The aqueous layer was neutralized with KOH until PH=6˜7. The white precipitate was filtered off to get a clear solution, which was extracted with ethyl acetate (600 mL×3). The combined organic layers were washed with brine twice, dried over anhydrous sodium sulfate. After filtration and evaporation, 8-5 (212.7 g, 100%) was obtained as brownish white solid.

後処理

  1. customThe volatiles were removed in vacuo
  2. customThe residue was quenched with cooled water (500 mL) and ethyl acetate (1.5 L)
  3. filtrationThe white precipitate was filtered off
  4. customto get a clear solution, which
  5. extractionwas extracted with ethyl acetate (600 mL×3)
  6. washThe combined organic layers were washed with brine twice
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationAfter filtration and evaporation

出典と根拠

ORDレコード
ord-a391756ec1f948629150018549acdcc5
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08912220B2

反応ノート

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