Phenyltrimethylammonium bromide dibromide → HCID 22473879, compound

HRID 2183637Notes

Reaction equation

HRID 2183637 reaction equation
[Br-:1].[Br-].[Br-].C1([N+](C)(C)C)C=CC=CC=1.C1([N+](C)(C)C)C=CC=CC=1.C1([N+](C)(C)C)C=CC=CC=1.[CH3:34][C:35]1[C:43]2[CH:42]=[C:41]([C:44](=[O:47])[CH2:45][CH3:46])[S:40][C:39]=2[CH:38]=[CH:37][CH:36]=1>O1CCCC1>[Br:1][CH:45]([CH3:46])[C:44]([C:41]1[S:40][C:39]2[CH:38]=[CH:37][CH:36]=[C:35]([CH3:34])[C:43]=2[CH:42]=1)=[O:47]

Participants

4

Conditions

Temperature
0 °C

Procedure

Phenyltrimethylammonium tribromide (1.47 g) was added in portions under nitrogen at 0° C. over 10 minutes to a stirred solution of 1-(4-methylbenzo[b]thiophen-2-yl)propan-1-one (0.53 g) in tetrahydrofuran (15 ml), then the mixture was stirred at 0° C. for 3 hours and at ambient temperature for 16 hours. Further phenyltrimethylammonium tribromide (0.49 g) was added, then the mixture was stirred at ambient temperature for 26 hours and filtered. The solvent was removed in vacuo and the residue was purified by flash chromatography over silica using a 4:1 mixture of petroleum ether (b.p. 60-80° C.) and dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to give 2-bromo-1-(4-methylbenzo[b]thiophen-2-yl)propan-1-one (0.3 g) as a yellow solid which was used without further purification.

Workup

  1. stirringthe mixture was stirred at ambient temperature for 26 hours
  2. filtrationfiltered
  3. customThe solvent was removed in vacuo
  4. customthe residue was purified by flash chromatography over silica using
  5. additiona 4:1 mixture of petroleum ether (b.p. 60-80° C.) and dichloromethane as eluant
  6. customthe solvents removed in vacuo

Sources & evidence

ORD record
ord-14686ca1372f4bce820308c7a14cba23
Source dataset
uspto-grants-2005_05
Patent number
US06900216B2

Reaction notes

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