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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271873Generated: October 26, 2026

Citric Acid → {2-[(5-Vinyl-benzofuran-2-carbonyl)-amino]-phenyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1271873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantDibutyl Vinylboronate (stabilized with Phenothiazine)HCID 236543—
ReactantSodium MethoxideHCID 10942334—
Reactant{2-[(5-Bromo-benzofuran-2-carbonyl)-amino]-phenyl}-carbamic acid tert-butyl esterHCID 69487214—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product{2-[(5-Vinyl-benzofuran-2-carbonyl)-amino]-phenyl}-carbamic acid tert-butyl esterHCID 6949002486%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 2027 mg (4.7 mmol) {2-[(5-Bromo-benzofuran-2-carbonyl)-amino]-phenyl}-carbamic acid tert-butyl ester (56) and 289 mg (0.25 mmol) Pd(Ph3)4 in 40 ml toluene were added 1.84 ml of a 5.4M solution of sodium methoxide in methanol and 957 mg (5.2 mmol) vinylboronic acid dibutyl ester and the solution was heated at 90° C. for 3 h. The reaction mixture was poured on 5% aqueous citric acid. Extraction with ethyl acetate, washing of the organic phase with brine. The organic phase was dried over sodium sulfate, the solvent was evaporated and the residue subjected to silica gel chromatography (petrolether/ethylacetate 2:1) to give 1530 mg (4.04 mmol) {2-[(5-Vinyl-benzofuran-2-carbonyl)-amino]-phenyl}-carbamic acid tert-butyl ester (57).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208491B2
Source datasetuspto-grants-2007_04
ORD IDord-2482a54683f845e787c19b6eb434933f
Source noteuspto-grants-2007_04