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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537984Generated: October 30, 2026

Potassium Bromide → Methyl 3'-bromo-4'-methoxy-2-methylbiphenyl-4-carboxylate

https://huagongshe.com/reaction/537984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantMethyl 4-(4-methoxyphenyl)-3-methylbenzoateHCID 67065985—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductMethyl 3'-bromo-4'-methoxy-2-methylbiphenyl-4-carboxylateHCID 67066022—

Reaction Steps

To a solution of methyl 4′-methoxy-2-methylbiphenyl-4-carboxylate (71.5 g, 0.279 mol) in acetonitrile (1.43 L) and water (572 mL) was added oxone (180.1 g, 0.293 mol). Then a solution of KBr (38.2 g, 0.321 mol) in water (143 mL) was slowly added over 30 minutes. The reaction was stirred for 2.5 hours, then water (715 mL) was added and the mixture was left standing for 1 hour. The solids were filtered and washed as follows: with a solution of MeCN/water (1:1, 350 mL, twice), water (700 mL, twice, then 350 mL) and dried to afford methyl 3′-bromo-4′-methoxy-2-methylbiphenyl-4-carboxylate. 1H NMR (CDCl3, 400 MHz) δ 7.94 (s, 1H), 7.89 (d, J=8.1 Hz, 1H), 7.53 (d, J=2.2 Hz, 1H), 7.3-7.2 (m, 2H), 6.97 (d, J=8.4 Hz, 1H), 3.96 (s, 3H), 3.94 (s, 3H), 2.32 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865707B2
Source datasetuspto-grants-2014_10
ORD IDord-716a866b4f204bf6a7d056ea3eba6101
Source noteuspto-grants-2014_10