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5-Bromo-2-nitro-9H-thioxanthene → HCID 59797442、化合物

HRID 33806
ノート
印刷プレビュー

反応式

HRID 33806 の反応式
[Br:1][C:2]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:3]=1[S:4][C:5]1[CH:6]=[CH:7][C:8]([N+:16]([O-])=O)=[CH:9][C:10]=1[CH2:11]2>C(O)(=O)C.[Zn]>[Br:1][C:2]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:3]=1[S:4][C:5]1[CH:6]=[CH:7][C:8]([NH2:16])=[CH:9][C:10]=1[CH2:11]2
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 1

HCID 597974365-Bromo-2-nitro-9H-thioxanthene

生成物 1

HCID 59797442HCID 59797442、化合物収率 102.6%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 176Acetic Acid溶媒

実験手順

Zn dust (34.87 g, 533 mmol) was added to a stirred solution of 5-bromo-2-nitro-9H-thioxanthene (28.64 g, 88.9 mmol) in glacial acetic acid (300 ml) at 0° C. (ice bath). After one hour the ice bath was removed and the solution was left to react overnight at room temperature. The mixture was filtered through a pad of Celite and washed with copious amount of dichloromethane and the filtrate was evaporated in vacuo. Water was added (800 ml) to the residue and the pH was adjusted to pH 8 by addition of concentrated ammonia (100 ml). The solid formed was filtered and dried in a vacuum desiccator to give the title compound (26.64 g) and was used without any further purification. m/z (LC-MS, ESP), RT=4.53 min, (M++1)=294-292, (1:1, bromine isotope ratio present)

後処理

  1. customAfter one hour the ice bath was removed
  2. waitthe solution was left
  3. customto react overnight at room temperature
  4. filtrationThe mixture was filtered through a pad of Celite
  5. washwashed with copious amount of dichloromethane
  6. customthe filtrate was evaporated in vacuo
  7. additionWater was added (800 ml) to the residue
  8. additionthe pH was adjusted to pH 8 by addition of concentrated ammonia (100 ml)
  9. customThe solid formed
  10. filtrationwas filtered
  11. customdried in a vacuum desiccator

出典と根拠

ORDレコード
ord-1b0d4fc123124ec2b947b4794a33e6ac
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07429660B2

反応ノート

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