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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190899Generated: October 29, 2026

Phosphoric Acid → HCID 10457147, compound

https://huagongshe.com/reaction/2190899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantSodium Phosphate, DibasicHCID 24203—
ReactantSodium HypochloriteHCID 23665760—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
ReactantHCID 46193335HCID 46193335—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 10457147HCID 1045714798%

Reaction Conditions

Temperature35 °C

Reaction Steps

10 g (0.06 moles) of radical 2,2,6,6-tetramethyl-1-piperidinyl-oxyl (TEMPO) and 1160 ml of an aqueous solution of 120 g (1 mole) of sodium dihydrogen phosphate and 180 g (1 mole) of disodium hydrogen phosphate are added in sequence to a suspension of 333 g (0.74 moles) of 1,8-dibenzyloxy-3-(hydroxymethyl)anthraquinone in 1660 ml of acetonitrile. The reaction mixture is heated to 35° C. and a solution of 167 g (1.5 moles) of sodium chlorite 80% in 513 ml of water is added dropwise in 40-50 minutes, maintaining the temperature around 35-40° C. 20 ml of aqueous sodium hypochlorite 10-12% are then dripped in and the reaction is heated to 60-65° C. for three hours. It is cooled to room temperature and 1400 ml of water are added. Phosphoric acid 85% is dripped in until reaching a pH of 2.8-3.2. The solid obtained is filtered and washed with water (350 ml×2). The damp product is dried at 50° C. at reduced pressure for 14-16 hours, providing 337 g (yield 98%) of crude dibenzylrhein.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324411B2
Source datasetuspto-grants-2012_12
ORD IDord-7c7e38ab63e947479fcd7c3f26e87702
Source noteuspto-grants-2012_12