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Azido(trimethyl)stannane → 5-(2-Bromo-4-chloro-6-fluoro-phenyl)-2H-tetrazole

HRID 2046569
Notes
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Reaction equation

HRID 2046569 reaction equation
[Br:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([F:11])[C:3]=1[C:4]#[N:5].[N:12]([Sn](C)(C)C)=[N+:13]=[N-:14]>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([F:11])[C:3]=1[C:4]1[N:12]=[N:13][NH:14][N:5]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 5104973Azido(trimethyl)stannaneHCID 585795372-Bromo-4-chloro-6-fluorobenzonitrile

Product 1

HCID 679792895-(2-Bromo-4-chloro-6-fluoro-phenyl)-2H-tetrazoleYield 88.7%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Conditions

Temperature
120 °C

Procedure

A mixture of 2-bromo-4-chloro-6-fluoro-benzonitrile (4 g, 17.06 mmol) and azidotrimethyltin (3.86 g, 18.77 mmol) in toluene (100 ml) was heated to 120° C. for 72 h. After completion of the reaction, the mixture was partitioned between EtOAc (50 ml) and aqueous 0.5N HCl solution (40 ml). The organic layer was separated, washed with water and brine, dried with Na2SO4 and concentrated under reduced pressure to afford the title compound (4.2 g, 87%) as red solid.

Workup

  1. customAfter completion of the reaction
  2. customthe mixture was partitioned between EtOAc (50 ml) and aqueous 0.5N HCl solution (40 ml)
  3. customThe organic layer was separated
  4. washwashed with water and brine
  5. dry with materialdried with Na2SO4
  6. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-894b472c4021436c95b35f1bcbdda3d0
Source dataset
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08592426B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes