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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428175Generated: October 29, 2026

Acetic Anhydride → n-[2-(3,4-Dihydro-2h-4-chromenyl)ethyl]acetamide

https://huagongshe.com/reaction/428175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium AcetateHCID 517045—
Reactant2-(Chroman-4-yl)acetonitrileHCID 13362781—
CatalystNickelHCID 935—
Productn-[2-(3,4-Dihydro-2h-4-chromenyl)ethyl]acetamideHCID 18177447—

Reaction Conditions

Temperature50 °C

Reaction Steps

The saturated cyano compound obtained in Step B is solubilized in the reactor of a Parr apparatus with acetic anhydride. Sodium acetate (1.5 eq.) and also Raney nickel (6 mg per 50 mg of product) are then introduced into the reaction medium. The whole is heated at 50° C. under hydrogen pressure of 40 psi for 12 hours. Once the solvent has been removed after returning to normal temperature and pressure conditions, extraction is carried out with ethyl acetate. Purification of the concentrated organic phase by flash chromatography (CHCl3/AcOEt 7/3) results in the desired amide. Colourless gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313160B1
Source datasetuspto-grants-2001_11
ORD IDord-c82db8a0e861465ab0d824918a33f986
Source noteuspto-grants-2001_11