Bromine → 5-Bromo-2,3-dihydro-1-benzothiophene

HRID 576364

Reaction equation

HRID 576364 reaction equation
[S:1]1[CH2:5][CH2:4][C:3]2[CH:6]=[CH:7][CH:8]=[CH:9][C:2]1=2.[Br:10]Br.C(=O)([O-])O.[Na+]>ClCCl.[Fe]>[Br:10][C:7]1[CH:8]=[CH:9][C:2]2[S:1][CH2:5][CH2:4][C:3]=2[CH:6]=1

Participants

6

Procedure

Iron powder (10.4 mg, 1.47 mmol) was added to a solution of 2,3-dihydrobenzo[b]thiophene 112 (400 mg, 2.94 mmol) in dichloromethane (5.9 mL). Bromine (0.15 mL, 2.94 mmol) was added dropwise to the mixture with stirring under ice-cooling. This mixture was stirred at the same temperature for 30 minutes. Saturated aqueous sodium hydrogen carbonate solution was added to the mixture and this was extracted with dichloromethane. The organic layer was washed with water, dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography to provide the desired product 113 (396 mg, 63%).

Workup

  1. temperaturecooling
  2. stirringThis mixture was stirred at the same temperature for 30 minutes
  3. extractionthis was extracted with dichloromethane
  4. washThe organic layer was washed with water
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-de53561b2d9d4ec9b30364aa21aeac86
Source dataset
uspto-grants-2015_05
Patent number
US09034921B2

Linked notes

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