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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751036Generated: October 30, 2026

Water → N-(7-Cyano-2,3-dihydrobenzofuran-4-yl)-acetamide

https://huagongshe.com/reaction/751036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant4-Acetylamino-2,3-dihydrobenzofuran-7-carboxylic acid amideHCID 68459409—
SolventTetrahydrofuranHCID 8028—
ProductN-(7-Cyano-2,3-dihydrobenzofuran-4-yl)-acetamideHCID 6845922371.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of compound 4A (3.5 g, 16 mmol) in THF (64 mL) at 0° C. under Ar was added pyridine (6.5 mL, 80 mmol), followed by trifluoroacetic anhydride (5.6 mL, 40 mmol) dropwise. After addition, the reaction mixture was stirred at 0° C. for 5 min, then pored into H2O (50 mL), extracted with EtOAc (3×100 mL). The combined EtOAc extracts were washed with brine, dried (Na2SO4), and concentrated under reduced pressure to give a crude product, which was purified by crystallization from MeOH-EtOAc-Hexane to furnish the title compound (2.3 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405234B2
Source datasetuspto-grants-2008_07
ORD IDord-c05ecb52b26743fa92032e02d713728c
Source noteuspto-grants-2008_07