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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199574Generated: October 31, 2026

Acetonitrile → Methyl 2-[2-(4-methanesulfonylphenyl)thiophen-3-yl]acetate

https://huagongshe.com/reaction/2199574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Methanesulfonyl)phenylboronic acidHCID 2734364—
ReactantMethyl 2-(2-bromothiophen-3-yl)acetateHCID 57116941—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductMethyl 2-[2-(4-methanesulfonylphenyl)thiophen-3-yl]acetateHCID 71230756—

Reaction Steps

Intermediate B (2.30 g, 9.78 mmol), 4-methylsulfonylphenylboronic acid (1.96 g, 9.78 mmol), K2CO3 (4.15 g, 30.0 mmol), tetrakis(triphenylphosphine)palladium(0) (150 mg, 0.130 mmol), MeCN (30 ml) and water (10 ml) were heated at 70° C. for 1 hour. The organic phase was removed in vacuo and the crude material was dissolved in DCM. The mixture was purified by flash chromatography using 30% and 50% EtOAc in iso-hexane as eluent. Yield: 2.25 g (74%); white solid. 1H NMR (400 MHz, CDCl3): δ 3.11 (s, 3H), 3.67 (s, 2H), 3.74 (s, 3H), 7.13 (d, J 5.0 Hz, 1H), 7.39 (d, J 5.0 Hz, 1H), 7.67-7.72 (m, 2H), 7.98-8.04 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359311B2
Source datasetuspto-grants-2016_06
ORD IDord-252277da2fb340068997b0fe1aaa8bbe
Source noteuspto-grants-2016_06