Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600473Generated: November 3, 2026

2,6-Dihydroxyanthraquinone → HCID 53655413, compound

https://huagongshe.com/reaction/1600473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DihydroxyanthraquinoneHCID 6776—
ReactantPotassium CarbonateHCID 11430—
ReactantDiethyl (4-bromobutyl)phosphonateHCID 14411016—
SolventDimethylformamideHCID 6228—
ProductHCID 53655413HCID 53655413—

Reaction Steps

2,6-dihydroxyanthraquinone (1.19 g, 4.98 mmol) and diethyl(4-bromobutyl)phosphonate (3.0 g, 10 mmol) were heated at 60 ° C. in 5 ml DMF in the presence of 0.8 g of K2CO3 for 72 hours. The solution was extracted with CH2Cl2. The CH2Cl2 solution was dried, leaving a yellow solid. The ester was purified by column chromatography. The bisphosphonate ester was converted to the acid by overnight stirring with 4-fold excess of bromotrimethylsilane in dry dichloromethane followed by addition of water. The bisphosphonic acid derivative was washed with CH2Cl2, filtered and collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05976486
Source datasetuspto-grants-1999_11
ORD IDord-ad4abfbcf9ae429c9f79a37c477e5d63
Source noteuspto-grants-1999_11