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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626134Generated: November 1, 2026

Trifluoroacetic anhydride → 8-Hydroxy-5,6,7,8-tetrahydroquinoline-3-carbonitrile

https://huagongshe.com/reaction/1626134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant3-Cyano-5,6,7,8-tetrahydroquinoline 1-oxideHCID 68227201—
Product8-Hydroxy-5,6,7,8-tetrahydroquinoline-3-carbonitrileHCID 6822714487.2%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of 3-cyano-5,6,7,8-tetrahydroquinoline 1-oxide (645 mg, 3.7 mmol) was added dropwise under ice cooling trifluoroacetic anhydride (6.22 g, 4.18 ml, 29.6 mmol). The light yellow solution was stirred at 23° C. for 18 h. The mixture was quenched with a solution of sodium hydroxide (1N) and stirred vigorously for 30 minutes, then extracted twice with dichloromethane. The combined organic layers were dried over sodium sulphate, filtered and evaporated. The residue was purified by silica gel flash chromatography with n-heptane/ethyl acetate to give the 8-hydroxy-5,6,7,8-tetrahydroquinoline-3-carbonitrile (562 mg, 87% yield) as a white solid. MS (ISP): m/z=175.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785436B2
Source datasetuspto-grants-2014_07
ORD IDord-eae47f4663bc4a60a4da66e288f0ca2c
Source noteuspto-grants-2014_07