Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109036Generated: October 31, 2026

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

https://huagongshe.com/reaction/1109036

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 numberUS05318994
Source datasetuspto-grants-1994_06
ORD IDord-619122b40cfe4024bc2ad68370cf8770
Source noteuspto-grants-1994_06