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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716006Generated: October 29, 2026

Sodium Carbonate → Methyl 3-bromobiphenyl-2-carboxylate

https://huagongshe.com/reaction/716006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantMethyl 2,6-dibromobenzoateHCID 817273—
SolventTolueneHCID 1140—
ProductMethyl 3-bromobiphenyl-2-carboxylateHCID 13352656—

Reaction Steps

A mixture of the product from Example 114A (2.2 g, 7.5 mmol), phenylboronic acid (919 mg, 7.5 mmol), sodium carbonate (7.55 mL, 2 M aqueous solution, 15.1 mmol) tetrakis(triphenyphosphine)palladium(0) (261 mg, 0.23 mmol) and 50 mL of toluene were refluxed for 16 hours under nitrogen. The reaction was cooled and partitioned between 50 mL of water and 50 mL of ethyl acetate. The aqueous portion was separated and extracted with 2×25 mL of ethyl acetate and the combined organic extracts were washed with 2×25 mL of water and 1×25 mL of brine and dried over sodium sulfate. The organic solution was concentrated and the residue was purified via flash chromatography on a silica gel column (95:5 hexane:ethyl acetate) to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 3.63 (s, 3H) 7.35-7.60 (m, 6H) 7.71-7.79 (m, 2H); MS (DCI+) m/z 308.0 [M+NH4]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187483B2
Source datasetuspto-grants-2015_11
ORD IDord-a7214b8699724064904a7ca49283ec19
Source noteuspto-grants-2015_11