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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451589Generated: October 25, 2026

Ammonia → 5-tert-butyl-2,3-dihydro-1H-inden-1-amine

https://huagongshe.com/reaction/451589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant5-tert-butyl-1-indanone O-methyloximeHCID 73047460—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5-tert-butyl-2,3-dihydro-1H-inden-1-amineHCID 11506601—

Reaction Conditions

Temperature50 °C

Reaction Steps

5-tert-Butyl-1-indanone O-methyloxime (4.37 g, 20.2 mmol) and 10% palladium on carbon (2.2 g) were combined in methanol (50 ml) and ammonia (10 ml) and placed in a Parr apparatus, which was charged with hydrogen to 60 psi. The reaction was shaken at 50° C. for 16 hours. The reaction mixture was filtered and the filtrate was evaporated under reduced pressure. The residue was treated with diethyl ether (100 ml) and extracted with hydrochloric acid (1N, 3×50 ml). The combined aqueous extracts were neutralized with sodium hydroxide (6 g) in water (25 ml) and extracted with diethyl ether. The organic extracts were combined, dried with magnesium sulfate, and the filtrate was evaporated under reduced pressure to provide the title compound, which was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487116B2
Source datasetuspto-grants-2013_07
ORD IDord-9e243e9d9646465aaec0cc424959d5bf
Source noteuspto-grants-2013_07