HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403248Generated: October 29, 2026
Acetic Acid → 5,6,7,8-Tetrahydroquinoline-3-carbonitrile
https://huagongshe.com/reaction/403248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrile | HCID 3779818 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,6,7,8-Tetrahydroquinoline-3-carbonitrile | HCID 593872 | 53% |
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 aqueous 1 M NaOH solution, filtered through Celite®, the filtrate extracted with THF, the organic layers dried over Na2SO4 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748418B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-6c4472b0e94243d7b8a936101137f053 |
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| Source note | uspto-grants-2014_06 |
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