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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 3-Cyano-5,6,7,8-tetrahydroquinoline 1-oxide | HCID 68227201 | — |
| Product | 8-Hydroxy-5,6,7,8-tetrahydroquinoline-3-carbonitrile | HCID 68227144 | 87.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785436B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-eae47f4663bc4a60a4da66e288f0ca2c |
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| Source note | uspto-grants-2014_07 |
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