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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantIsopropylamineHCID 6363—
Reactant9-Carbamoyl-9-(3-oxobutyl)fluoreneHCID 13853488—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDiethyl EtherHCID 3283—
Product9-Carbamoyl-9-(3-isopropylaminobutyl)fluoreneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04658061
Source datasetuspto-grants-1987_04
ORD IDord-46f935dd6df740969ea664a64977405e
Source noteuspto-grants-1987_04