Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026359Generated: November 1, 2026

Acetic Anhydride → HCID 67777582, compound

https://huagongshe.com/reaction/1026359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 67777689HCID 67777689—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
SolventSodium HydroxideHCID 14798—
ProductHCID 67777582HCID 67777582—

Reaction Steps

A solution of acetic anhydride (0.126 mL) was added dropwise to a solution of diastereomer of 2-(5-{[(2S)-2-aminopropyl]oxy}pyridin-2-yl)-2-methyl-2,3-dihydro-1-benzofuran-6-ol (500 mg) in pyridine (15 mL) at ambient temperature. After being stirred at ambient temperature for 2 hr, the mixture was diluted with methanol (15 mL) and 4 M sodium hydroxide (10 mL). The mixture was stirred at ambient temperature for 15 hr. The organic solvent was removed under reduced pressure, and the aqueous solution was acidified with 4 M hydrochloric acid and extracted with ethyl acetate. The organic layer was separated, washed with water and brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (350 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729102B2
Source datasetuspto-grants-2014_05
ORD IDord-2a5aa607c43649c6ad8db878ddf4a8e3
Source noteuspto-grants-2014_05