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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626132Generated: November 3, 2026

Acetic Acid → 5,6,7,8-Tetrahydroquinoline-3-carbonitrile

https://huagongshe.com/reaction/1626132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrileHCID 3779818—
ReactantSodium Acetate TrihydrateHCID 23665404—
CatalystZincHCID 23994—
SolventWaterHCID 962—
Product5,6,7,8-Tetrahydroquinoline-3-carbonitrileHCID 59387253%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of commercially available 2-chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrile [CAS no 65242-27-5] (1 g, 5.19 mmol), zinc dust (activated) (602 mg, 9.2 mmol) and sodium acetate trihydrate (694 mg, 479 μl, 5.1 mmol) in acetic acid (5.19 g, 4.95 ml, 86.4 mmol) was stirred at 60° C. for 2 hours. Water (2.5 ml) was added and the mixture stirred at 60° C. for another 5 hours. After cooling to 23° C., the mixture was basified with an aqueous solution of sodium hydroxide (1M) and filtered through Celite®. The filtrate was extracted with tetrahydrofuran, the organic layers dried over sodium sulphate and the solvent evaporated leaving a yellow liquid. The crude material was purified by silica gel flash chromatography with n-heptane/ethyl acetate to give the 5,6,7,8-tetrahydroquinoline-3-carbonitrile as a white solid (433 mg, 53% yield). MS (ISP): m/z=159.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785436B2
Source datasetuspto-grants-2014_07
ORD IDord-950be0627e4947a2b0bd54916f5250ac
Source noteuspto-grants-2014_07