HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898745Generated: October 29, 2026
Hydrochloric Acid → 1,2,3,3a,4,8b-Hexahydrocyclopenta[b]indole
https://huagongshe.com/reaction/898745
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,2,3,4-Tetrahydro-cyclopenta(b)indole | HCID 270305 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 1,2,3,3a,4,8b-Hexahydrocyclopenta[b]indole | HCID 21873574 | 69.1% |
Reaction Steps
A mixture of 1,2,3,4-tetrahydrocyclopenta[b]indole (11 mmol, 1.8 g), 5% Pd/C (0.5 g), and concentrated hydrochloric acid (1.2 mL) was hydrogenated at 45 psi on a Parr shaker. After 3 h, the mixture was removed from the shaker and filtered through Celite. The solid bed was washed with methanol. The filtrate was concentrated. The crude oil was dissolved in 1 N HCl and washed with ether. The aqueous phase was treated with 2.5 N NaOH to pH>10 and then extracted with chloroform. The combined chloroform extracts were dried over MgSO4, filtered and concentrated to give the crude indoline. The material was purified by flash column chromatography through silica gel (Biotage, elution with 10% ethyl acetate-hexanes) to give the known indoline (7.6 mmol, 1.2 g, 69%) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07351839B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-97a61d1ab04f4d4282a7c206923c4eb6 |
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| Source note | uspto-grants-2008_04 |
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