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Sodium Azide → 1-(Azidomethyl)-4-fluoro-2-iodobenzene

HRID 1664184
Notes
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Reaction equation

HRID 1664184 reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([F:9])=[CH:5][C:4]=1[I:10].[N-:11]=[N+:12]=[N-:13].[Na+]>CN(C)C=O>[N:11]([CH2:2][C:3]1[CH:8]=[CH:7][C:6]([F:9])=[CH:5][C:4]=1[I:10])=[N+:12]=[N-:13]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 33557Sodium AzideHCID 128060541-(Bromomethyl)-4-fluoro-2-iodobenzene

Product 1

HCID 210697761-(Azidomethyl)-4-fluoro-2-iodobenzeneYield 99.8%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
50 °C

Procedure

A solution of 1-(bromomethyl)-4-fluoro-2-iodobenzene (M. Protiva et al., Collect. Czech. Chem. Comm., 44, 1979, 2108-2123) (17.9 g, 56.8 mmol) in N,N-dimethylformamide (35 ml) was treated with sodium azide (5.0 g, 76.7 mmol) and the resulting mixture was heated to 50° C. for 4 h. The cooled mixture was filtered, the filtrate was concentrated in vacuo and the residue was chromatographed on silica gel (elution hexane) to give 15.7 g (97% yield) of the title azide as a clear oil. 1HNMR 400 MHz (DMSO-d6) δ: 4.53 (2H, s), 7.32 (1H, m), 7.54 (1H, dd, J=6.0, 8.6 Hz), 7.83 (1H, dd, J=3.0, 8.0 Hz).

Workup

  1. filtrationThe cooled mixture was filtered
  2. concentrationthe filtrate was concentrated in vacuo
  3. customthe residue was chromatographed on silica gel (elution hexane)

Sources & evidence

ORD record
ord-8b41232356e4455d93ec86a85627ba20
Source dataset
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08039458B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes