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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593936Generated: November 1, 2026

Sodium Hydroxide → 2,7-Diaminoacridin-9(10H)-one

https://huagongshe.com/reaction/1593936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium sulfide nonahydrateHCID 73972—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-7-nitroacridin-9(10H)-oneHCID 21074080—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2,7-Diaminoacridin-9(10H)-oneHCID 2107407994.1%

Reaction Steps

See Bogert et al., 1930. To a stirred suspension of 2-amino-7-nitro-9(10H)-acridone 11 (22.5 g, 88.2 mmol) in ethanol was added, in one lot, a solution of sodium sulphide nonahydrate (94.5 g, 0.394 mol) and sodium hydroxide (37.5 g, 0.938 mol) in water (1.625 L). The mixture was refluxed with stirring for 16 hr. On cooling, saturated sodium bicarbonate solution (250 mL) was added and the total volume of the mixture reduced to 700 mL on a rotary evaporator. The flask was chilled in ice for 3 hr after which the product was collected on a glass sinter. The product was washed with water (4×200 mL) followed by ice-cold ethanol (2×100 mL), dry ether (2×100 mL) and finally hexane (2×100 mL). The product, 12, was dried over P2O5 under vacuum to yield an olive-green solid (18.70 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300930B2
Source datasetuspto-grants-2007_11
ORD IDord-3c5cdcdec7dd46c8965615e8165eba32
Source noteuspto-grants-2007_11