Ethanol → Ethyl 2-(3-bromo-4-hydroxyphenyl)acetate
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([OH:12])=[O:11])[CH:5]=[CH:6][C:7]=1[OH:8].S(=O)(=O)(O)O.[CH3:18][CH2:19]O>>[CH2:18]([O:11][C:10](=[O:12])[CH2:9][C:4]1[CH:5]=[CH:6][C:7]([OH:8])=[C:2]([Br:1])[CH:3]=1)[CH3:19]Participants
4
Procedure
(3-Bromo-4-hydroxy-phenyl)-acetic acid (5.6 mmol) in EtOH (20 mL) was treated with sulfuric acid (1 mL) and stirred at room temperature over the weekend. The mixture was concentrated to give the title compound.
Workup
- concentrationThe mixture was concentrated
Sources & evidence
- ORD record
- ord-434516121a0b4996ae885f5f0b5347c6
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08067445B2
Reaction notes
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