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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378168Generated: October 25, 2026

Hydrochloric Acid → Methyl 3-bromo-5-iodobenzoate

https://huagongshe.com/reaction/378168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromo-5-iodobenzoic acidHCID 5182520—
SolventMethanolHCID 887—
ProductMethyl 3-bromo-5-iodobenzoateHCID 21942573—

Reaction Steps

Methanol (40 mL) was added to a 250 mL round bottom flask followed by 60 mL of a solution saturated with anhydrous hydrochloric acid. 3-bromo-5-iodobenzoic acid (Aldrich)(5.02 g, 0.015 mole) was then added and the reaction mixture was stirred at room temperature for 6 hours. The reaction mixture was poured into chilled saturated NaHCO3 solution (700 mL). The mixture was extracted 3× with methylene chloride (100 mL). The organic layers were combined, dried over MgSO4 and concentrated under vacuum to yield methyl-5-bromo-3-iodobenzoate (5.08 g) as a pink solid. MP=55-57° C. MS and NMR were consistent with the desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028223
Source datasetuspto-grants-2000_02
ORD IDord-f3727634fd1140869e6dabd58759f31a
Source noteuspto-grants-2000_02