HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Thiophene → HCID 12060894, compound

HRID 1588005
Notes
Print preview

Reaction equation

HRID 1588005 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][CH:8]=1)N.C(ON=O)CC(C)C.[S:17]1[CH:21]=[CH:20][CH:19]=[CH:18]1>CCOCC>[Br:1][C:2]1[CH:3]=[C:4]([C:18]2[S:17][CH:21]=[CH:20][CH:19]=2)[CH:6]=[CH:7][CH:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8030ThiopheneHCID 8053Isoamyl NitriteHCID 115623-Bromoaniline

Product 1

HCID 12060894HCID 12060894, compoundYield 34%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

To a stirred solution of m-bromoaniline (34.4 g; 0.2M) in thiophene (200 mL) was added isoamylnitrite (46.86 g; 0.4M) dropwise over a period of 30 mins. at 0° C. The resulting mixture was cautiously warmed to R.T. and heated to reflux for 16 hours. The reaction mixture was cooled, diluted with 400 mL of ether, washed with 3×100 mL of satd. sodium chloride solution, and dried over anhydrous magnesium sulfate. Solvent and excess thiophene were removed. A solution of the residue in 200 mL of ether was filtered through 50 G silica gel bed. Solvent was removed, and the residue was distilled to give 34% of 2-(3'-bromophenyl)thiophene as a yellow liquid boiling at 130°-2°/~0.2 mm. This liquid solidified on standing in the refrigerator.

Workup

  1. customat 0° C
  2. temperatureheated
  3. temperatureto reflux for 16 hours
  4. temperatureThe reaction mixture was cooled
  5. washwashed with 3×100 mL of satd
  6. dry with materialsodium chloride solution, and dried over anhydrous magnesium sulfate
  7. customSolvent and excess thiophene were removed
  8. filtrationA solution of the residue in 200 mL of ether was filtered through 50 G silica gel bed
  9. customSolvent was removed
  10. distillationthe residue was distilled

Sources & evidence

ORD record
ord-d869d74957a0467b84b53c6e794ee9f7
Source dataset
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05220011

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes