HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384397Generated: October 30, 2026
Bromine → Ethyl 3′-bromo-4′-methoxy[1,1′-biphenyl]-4-carboxylate
https://huagongshe.com/reaction/1384397
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethyl 4'-methoxy[1,1'-biphenyl]-4-carboxylate | HCID 2764348 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Ethyl 3′-bromo-4′-methoxy[1,1′-biphenyl]-4-carboxylate | HCID 85749597 | — |
Reaction Steps
A solution of bromine (14.6 g, 91.3 mmol) in carbon tetrachloride (100 mL) is added to a stirred mixture of 4′-Methoxy-[1,1′-biphenyl]-4-carboxylic acid, ethyl ester (23.4 g, 91.3 mmol) and silica gal (100 g of particle size 0.040-0.063 mm: Merck 1.09385) in carbon tetrachloride (350 mL). The mixture is stirred at 20° C. for 4 h after which the silica gel is removed by filtration. The filtrate is washed with aqueous sodium hydrogen carbonate (200 mL of 1 M) followed by aqueous sodium thiosulphate (50 mL of 2 M), dried (Na2SO4), filtered and evaporated to dryness under reduced pressure to give the crude product which is recrystallised from ether-cyclohexane to give 3′-bromo-4′-methoxy-[1,1′-biphenyl]-4-carboxylic acid, ethyl ester as a colourless crystalline solid, m.p. 114-115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258843B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-3820fd2f66a848cbaaeb66fb3eadbf11 |
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| Source note | uspto-grants-2001_07 |
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