Bromotrimethylsilane → 2-Bromo-4-(trifluoromethyl)pyridine

HRID 1261660Notes

Reaction equation

HRID 1261660 reaction equation
Cl[C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][N:3]=1.[Br:12][Si](C)(C)C>C(#N)CC>[Br:12][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][N:3]=1

Participants

4

Procedure

A mixture of 2-chloro-4-(trifluoromethyl)pyridine (2.70 g, 14.9 mmol) and bromotrimethylsilane (3.90 mL, 29.6 mmol) in propanenitrile (15.0 mL) was heated under reflux for 22 h. The product (very volatile) was carefully rotary evaporated to give 4.07 g (propanenitrile contained) of thick light brown suspension w/o further purification. LC-MS calculated for C6H3BrF3N (M+H) 226.9; found 225.9/227.8.

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for 22 h
  3. customThe product (very volatile) was carefully rotary evaporated
  4. customto give
  5. custom4.07 g (propanenitrile contained) of thick light brown suspension w/o further purification

Sources & evidence

ORD record
ord-ea5c5b3f41744716858396370b96c3e7
Source dataset
uspto-grants-2013_06
Patent number
US08470827B2

Reaction notes

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