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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345136Generated: October 28, 2026

Hydrochloric Acid → 2,3-dihydro-1-octylamino-4,6-dimethyl-7-hydroxy-1H-indene hydrochloride

https://huagongshe.com/reaction/345136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-ChlorooctaneHCID 8142—
ReactantTriethylamineHCID 8471—
ReactantHCID 12857262HCID 12857262—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
Product2,3-dihydro-1-octylamino-4,6-dimethyl-7-hydroxy-1H-indene hydrochlorideHCID 1365591815.1%

Reaction Steps

To a solution containing 1.77 g of 1-amino-2,3-dihydro-4,6-dimethyl-7-hydroxy-1H-indene and 2 ml of triethylamine in 100 ml of chloroform was added dropwise 2.23 g of octyl chloride at room temperature. Then the reaction micture was stirred at the same temperature for 4 hours. The reaction mixture was washed with a diluted hydrochloric acid, water, an aqueous solution saturated with sodium bicarbonate, water and an aqueous soluction saturated with sodium chloride in this order, then dried with anhydrous sodium sulfate. The solvent was removed by evaporation and the residue thus obtained was dissolved in ethanol, tna an ethanol saturated with hydrogen chloride gas was added thereto form a hydrochlodide. Recrysttallized form acetonitrile to obtain 0.49 g of 2,3-dihydro-1-octylamino-4,6-dimethyl-7-hydroxy-1H-indene hydrochloride. Colorless needle-like crystals. Melting point: 120°-121° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055474
Source datasetuspto-grants-1991_10
ORD IDord-5c393ffbbf5f4ea1ae77778299073b47
Source noteuspto-grants-1991_10