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5-Bromo-2-nitro-9H-thioxanthene → HCID 59797442, 화합물

HRID 33806
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HRID 33806 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

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

생성물 1

HCID 59797442HCID 59797442, 화합물수율 102.6%

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

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)

후처리

  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

출처 및 근거

ORD 기록
ord-1b0d4fc123124ec2b947b4794a33e6ac
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07429660B2

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