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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969139Generated: October 27, 2026

Sodium Carbonate → Methyl 4-bromo-5-(4-benzyloxy-3-cyanophenyl)-3-fluorothiophene-2-carboxylate

https://huagongshe.com/reaction/1969139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 4,5-dibromo-3-fluorothiophene-2-carboxylateHCID 15533893—
Reactant[4-(Benzyloxy)-3-cyanophenyl]boronic acidHCID 66995507—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductMethyl 4-bromo-5-(4-benzyloxy-3-cyanophenyl)-3-fluorothiophene-2-carboxylateHCID 66995012—

Reaction Steps

(4-Benzyloxy-3-cyanophenyl)boronic acid and methyl 4,5-dibromo-3-fluorothiophene-2-carboxylate were dissolved in a mixed solution of toluene and a 1M aqueous sodium carbonate solution and the whole was heated at 110° C. for 2.5 days in the presence of tetrakis(triphenylphosphine)palladium to obtain methyl 4-bromo-5-(4-benzyloxy-3-cyanophenyl)-3-fluorothiophene-2-carboxylate. Methyl 4-bromo-5-(4-benzyloxy-3-cyanophenyl)-3-fluorothiophene-2-carboxylate and triethylamine were stirred at room temperature in 1,4-dioxane under a hydrogen atmosphere at normal pressure in the presence of palladium-carbon to obtain methyl 5-(3-cyano-4-hydroxyphenyl)-3-fluorothiophene-2-carboxylate. FN: 276.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426453B2
Source datasetuspto-grants-2013_04
ORD IDord-bef9fa3135f84e1a94092db78e93021b
Source noteuspto-grants-2013_04