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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751490Generated: October 30, 2026

Ammonium Hydroxide → 2-{4-[2-(Tetrahydropyran-2-yloxy)ethoxy]benzofur-7-yl}acetamide

https://huagongshe.com/reaction/751490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant{4-[2-(Tetrahydropyran-2-yloxy)ethoxy]benzofur-7-yl}acetic acidHCID 69270245—
SolventTetrahydrofuranHCID 8028—
Product2-{4-[2-(Tetrahydropyran-2-yloxy)ethoxy]benzofur-7-yl}acetamideHCID 6926769280%

Reaction Conditions

Temperature0 °C

Reaction Steps

Combine {4-[2-(Tetrahydropyran-2-yloxy)ethoxy]benzofur-7-yl}acetic acid (0.920 g, 2.872 mmol), and 1,1-carbonyldiimidazole (2.365 g, 14.585 mmol) in tetrahydrofuran (15 ml), and stir for 1 hour under nitrogen. Cool the mixture to 0° C., and add concentrated aqueous ammonium hydroxide (2 ml). Remove the ice bath, and stir the mixture at room temperature for 16 hours. Dilute the mixture with ethyl acetate, wash with water and brine, dry over sodium sulfate, filter, and concentrate. Purification using flash chromatography and eluting with hexane:ethyl acetate gives 0.732 g (80%) of the title product as a white solid. Mass spectrum: electrospray (m/z) 236 (M++1-85).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405305B2
Source datasetuspto-grants-2008_07
ORD IDord-16215c1e28164e1996bddbb55146c962
Source noteuspto-grants-2008_07