Nitrogen → 2-Bromo-4-chloro-1-methylthiobenzene

HRID 992485Notes

Reaction equation

HRID 992485 reaction equation
F[B-](F)(F)F.[Br:6][C:7]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:8]=1[N+]#N.[CH3:16][S-:17].[Na+].N#N>CC#N>[Br:6][C:7]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:8]=1[S:17][CH3:16]

Participants

5

Conditions

Temperature
23 °C

Procedure

A cold (0° C.) solution of 2-bromo-4-chlorobenzenediazonium tetrafluoroborate (5.0 g, 16.3 mmol) in CH3CN (50 mL) was treated portion wise with sodium thiomethoxide (1.15 g, 16.4 mmol) and a strong evolution of gas (N2) was observed. The mixture was warmed up to 23° C., stirred for 0.25 hours and filtered. The filtrate was concentrated in vacuo; the residue was taken up in CH2Cl2, stirred and the solution was then filtered. The CH2Cl2 filtrate was concentrated in vacuo affording a brown syrup that was distilled under vacuum to provide the purified title compound; bp 125° C./0.4 mm, 1.4 g, 37%. 1H NMR (CDCl3) δ7.56 (d, J=2.5 Hz, H-3, 1H), 7.30 (dd, J=2.5 Hz, J=8.6 Hz, H-5, 1H), 7.07 (d, J=8.6 Hz, H-6, 1H), 2.49 (s, CH3, 3H). IR 1569, 1544, 1450, 1434, 1371,1248, 1105, 1024, 868, 803, 784 cm31 1. Anal. Calcd. for C7H6BrClS: C, 35.39; H, 2.55. Found: C, 34.89; H, 2.51.

Workup

  1. filtrationfiltered
  2. concentrationThe filtrate was concentrated in vacuo
  3. stirringstirred
  4. filtrationthe solution was then filtered
  5. concentrationThe CH2Cl2 filtrate was concentrated in vacuo
  6. customaffording a brown syrup that
  7. distillationwas distilled under vacuum
  8. customto provide the
  9. custompurified title compound

Sources & evidence

ORD record
ord-f4e129f2faef4bccafa864a8f65373a1
Source dataset
uspto-grants-2002_10
Patent number
US06469042B1

Reaction notes

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