1-Bromo-7-nitro-thianthrene → 6-Bromo-thianthren-2-ylamine

HRID 33791ノート

反応式

HRID 33791 の反応式
[Br:1][C:2]1[C:15]2[S:14][C:13]3[C:8](=[CH:9][C:10]([N+:16]([O-])=O)=[CH:11][CH:12]=3)[S:7][C:6]=2[CH:5]=[CH:4][CH:3]=1>C(O)(=O)C.[Zn]>[Br:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:15]=1[S:14][C:13]1[CH:12]=[CH:11][C:10]([NH2:16])=[CH:9][C:8]=1[S:7]2

参加物

4

反応物 1

HCID 597974311-Bromo-7-nitro-thianthrene

生成物 1

HCID 597974306-Bromo-thianthren-2-ylamine収率 104%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 176Acetic Acid溶媒

実験手順

Zn dust (144.1 g, 2.2 mol) was added to a stirred solution of 1-bromo-7-nitro-thianthrene (125 g, 367.4 mmol) in glacial acetic acid (500 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 (500 ml) to the residue and the pH was adjusted to pH 8 by addition of concentrated ammonia. The solid formed was filtered and dried in a vacuum desiccator to give the title compound (118.5 g) and was used without any further purification. m/z (LC-MS, ESP), RT=4.92, (M++1)=310-312 (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 (500 ml) to the residue
  8. additionthe pH was adjusted to pH 8 by addition of concentrated ammonia
  9. customThe solid formed
  10. filtrationwas filtered
  11. customdried in a vacuum desiccator

出典と根拠

ORDレコード
ord-8ef930c0e2344088b06312cac3797f1e
出典データセット
uspto-grants-2008_09
特許番号
US07429660B2

反応ノート

読み込み中…