HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500452Generated: October 25, 2026
Sodium borohydride → 2-Cyclopentyl-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/500452
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Cyclopentylquinoline | HCID 21826432 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Cyclopentyl-1,2,3,4-tetrahydroquinoline | HCID 65041828 | 92.1% |
Reaction Steps
To a solution of 2-cyclopentylquinoline (7.95 g, 40.3 mmol) and nickel (II) chloride hexahydrate (1.63 g, 6.85 mmol) in methanol (120 ml) cooled in an ice/methanol bath was added sodium borohydride (6.1 g, 161.2 mmol) portionwise over 1.5 h. The cooling bath was removed and the reaction stirred for a further 30 minutes. The methanol was then removed in vacuo. To the resulting black precipitate was added 2 M hydrochloric acid (100 ml) and then basified with 10 M potassium hydroxide. The mixture was poured into a separating funnel and extracted with ether (4×200 ml). The combined organic layers were dried (MgSO4), filtered and the solvent removed in vacuo to give 2-cyclopentyl-1,2,3,4-tetrahydroquinoline (7.45 g, 37.1 mmol) as a light brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772227B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-3f234ec8a24c428ebc70d0e2e9896d2f |
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| Source note | uspto-grants-2010_08 |
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