HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542641Generated: October 26, 2026
Ethanol → 9-Carbamoyl-9-(3-isopropylaminobutyl)fluorene
https://huagongshe.com/reaction/542641
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | 9-Carbamoyl-9-(3-oxobutyl)fluorene | HCID 13853488 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 9-Carbamoyl-9-(3-isopropylaminobutyl)fluorene | HCID 13853492 | — |
Reaction Steps
A solution of 2.35 g. of 9-carbamoyl-9-(3-oxobutyl)fluorene from Example 2 in 200 ml. of ethanol containing 59.0 g. of isopropylamine and 2.0 g. of 5% palladium on charcoal was stirred for sixteen hours at 25° C. under 60 psi of hydrogen. The reaction mixture was filtered and the filtrate was concentrated to a volume of about 50 ml. The mixture was added to 200 ml. of diethyl ether and extracted with 6N hydrochloric acid. The aqueous acid extract was cooled, made alkaline by addition of 10% aqueous sodium hydroxide, and the alkaline solution was extracted several times with diethyl ether. The ethereal extracts were combined, washed with water, dried and the solvent was removed by evaporation under reduced pressure to provide a solid. The solid was dissolved in fresh diethyl ether and hydrogen chloride was bubbled into the solution. The precipitated crystals which formed were collected by filtration, dried and identified as 829 mg. of 9-carbamoyl-9-(3-isopropylaminobutyl)fluorene hydrochloride. m.p. 204°-206° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04658061 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-46f935dd6df740969ea664a64977405e |
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| Source note | uspto-grants-1987_04 |
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