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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483393Generated: October 25, 2026

Triethylamine → 2-(7-Methoxynaphthalen-1-yl)acetonitrile

https://huagongshe.com/reaction/483393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant2-(7-Methoxynaphthalen-1-yl)acetamideHCID 15149127—
SolventTetrahydrofuranHCID 8028—
Product2-(7-Methoxynaphthalen-1-yl)acetonitrileHCID 11264068—

Reaction Steps

The (7-methoxynaphth-1-yl)acetamide obtained in Stage E is suspended in 80 ml of anhydrous THF, and triethylamine is added. The solution is cooled in an ice bath, and then trifluoroacetic anhydride is added dropwise with magnetic agitation. Agitation is continued for one hour at room temperature. Then the mixture is dried and the residue taken up in water. The precipitate which forms is spun down, dried and recrystallized in isopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05225442
Source datasetuspto-grants-1993_07
ORD IDord-0d8297132e0147d980039df82d6e1541
Source noteuspto-grants-1993_07