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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394668Generated: October 30, 2026

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

https://huagongshe.com/reaction/394668

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 solubilised 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 numberUS06602903B2
Source datasetuspto-grants-2003_08
ORD IDord-bd5f294836f9440b91abffe41978c449
Source noteuspto-grants-2003_08