HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424788Generated: October 30, 2026
Hydrogen Bromide → HCID 66704062, compound
https://huagongshe.com/reaction/424788
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 66704060 | HCID 66704060 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | HCID 66704062 | HCID 66704062 | 31% |
Reaction Steps
To a solution of sodium nitrite (1.40 g) in dimethyl sulfoxide (50 mL) is added 2′-amino-4′-methoxy-biphenyl-4-carboxylic acid methyl ester (2.61 g). After 5 minutes, the reaction mixture is treated with a solution of 4.7 mL hydrobromic acid (48%) in 50 mL dimethyl sulfoxide. The reaction is allowed to stir at room temperature for 2 h. The reaction mixture is diluted with a solution of 20.0 g potassium carbonate dissolved in 400 mL water. The product is extracted five times with methylene chloride. The combined organic layers are dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue is chromatographed eluting with hexanes/ethyl acetate (99:1 to 86:14) to give 2′-bromo-4′-methoxy-biphenyl-4-carboxylic acid methyl ester (1.00 g, 31%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106077B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-b18ce641af084999befb95e1084cf6bf |
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| Source note | uspto-grants-2012_01 |
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