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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331227Generated: October 26, 2026

O-Phenylenediamine → HCID 68704972, compound

https://huagongshe.com/reaction/331227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-(1,2,2a,3,4,5-Hexahydroacenaphthylen-1-yl)piperidin-4-oneHCID 68706671—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 68704972HCID 6870497285.2%

Reaction Steps

To a cooled (0° C.) solution of 1-(1,2,2a,3,4,5-hexahydroacenaphthylen-1-yl)piperidin-4-one (1.00 g, 3.92 mmol) and 1,2-phenylenediamine (642 mg) in dichloroethane (30 ml) were added sodium triacetoxyborohydride (1.99 g) and acetic acid (0.509 ml), and the mixture was stirred at room temperature for 19 hr. The reaction mixture was poured into water, and the mixture was neutralized with potassium carbonate, and extracted with chloroform. The extract was washed with water and saturated brine, dried over sodium sulfate, and concentrated. The obtained residue was purified by silica gel column chromatography (chloroform/methanol) to give N-[1-(1,2,2a,3,4,5-hexahydroacenaphthylen-1-yl)piperidin-4-yl]-benzene-1,2-diamine (1.16 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877779B2
Source datasetuspto-grants-2014_11
ORD IDord-c4558bebad384ff8a7c6d7786f699d6c
Source noteuspto-grants-2014_11