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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051428Generated: October 31, 2026

Water → 5,7-Dimethyl-8-hydroxy-9-methylamino-1,2,3,4,4a,9a-hexahydrofluorene

https://huagongshe.com/reaction/2051428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethylamineHCID 6329—
ReactantSodium borohydrideHCID 4311764—
Reactant5,7-Dimethyl-8-hydroxy-1,2,3,4,4a,9a-hexahydro-9-fluorenoneHCID 15157183—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product5,7-Dimethyl-8-hydroxy-9-methylamino-1,2,3,4,4a,9a-hexahydrofluoreneHCID 15157247—

Reaction Steps

3.4 Milliliters of a methanol solution of 40% methylamine was added to a methanol solution containing 2 g of 5,7-dimethyl-8-hydroxy-1,2,3,4,4a,9a-hexahydro-9-fluorenone in 20 ml of methanol and the mixture was refluxed under heating for 4 hours. Then, thereto were further added 10 ml of methanol and 3.4 ml of a methanol solution of 40% methyl amine, followed by refluxing for 6 hours. After left to stand for cooling, 3.66 g of sodium borohydride was gradually added thereto with stirring at room temperature, followed by stirring for 1 hour at the same temperature. Then, water was added to the reaction mixture and extraction was effected with chloroform. The organic layer was dried with magnesium sulfate and then the solvent was distilled off. The residue was purified by a silica gel column chromatography (eluent: ethyl acetate:n-hexane=1:1) and then recrystallized from ethanol to obtain 0.70 g of 5,7-dimethyl-8-hydroxy-9-methylamino-1,2,3,4,4a,9a-hexahydrofluorene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05017724
Source datasetuspto-grants-1991_05
ORD IDord-d11e0f12b3dc414c8fefa5f65961fe20
Source noteuspto-grants-1991_05