1-Bromo-4-[(2,2-dimethoxyethyl)sulfanyl]benzene → 5-Bromo-1-benzothiophene
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH2:9][CH:10](OC)OC)=[CH:4][CH:3]=1>ClC1C=CC=CC=1>[Br:1][C:2]1[CH:7]=[CH:6][C:5]2[S:8][CH:9]=[CH:10][C:4]=2[CH:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of polyphosphoric acid (10 g) in chlorobenzene (260 mL) was heated to reflux and added, under nitrogen, dropwise in one hour 1-bromo-4-(2,2-dimethoxy-ethylsulfanyl)-benzene (compound PRE12; 9.71 g, 35 mmol). The reaction mixture was then heated for 4 h until reaction is complete, cooled, quenched with water (150 mL) and extracted into methylene chloride. Combined organic layer was dried over Na2SO4 and concentrated to give a crude residue that was purified by flash chromatography (silica, eluting solvent: petroleum ether) to give 3.8 g of 5-bromo-benzo[b]thiophene (white solid) (Yield=51%).
Workup
- temperaturewas heated
- temperatureto reflux
- temperatureThe reaction mixture was then heated for 4 h until reaction
- temperaturecooled
- customquenched with water (150 mL)
- extractionextracted into methylene chloride
- dry with materialCombined organic layer was dried over Na2SO4
- concentrationconcentrated
- customto give a crude residue that
- customwas purified by flash chromatography (silica, eluting solvent: petroleum ether)
Sources & evidence
- ORD record
- ord-f9571fdaf4c64417a23cc8e34b34d902
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07449481B2
Reaction notes
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