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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578610Generated: October 31, 2026

HCID 11759759, compound → HCID 89630158, compound

https://huagongshe.com/reaction/578610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11759759HCID 11759759—
ReactantHCID 15153821HCID 15153821—
ReactantHCID 178418250HCID 178418250—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 89630158HCID 8963015890%

Reaction Steps

KOCN (3.33 g, 41.0 mmol, 5.85 eq.) and Bu4NBr (1.77 g, 5.49 mmol, 0.8 eq.) were added to a solution of the 10-bromodecylmethacrylate from the 1st step (8.36 g, 27.4 mmol, 3.9 eq.) in anhydrous acetonitrile (55 ml) and the reaction mixture was stirred for 64 h. The reaction mixture was subsequently concentrated in vacuo and hexane (100 ml) was added. After filtration of the obtained solution and concentrating in vacuo 4.75 g of a yellow oil was obtained. To this oil a solution of 2-hydroxymethyl-1,3-propylene-bisphosphonic acid tetraethylester (2.41 g, 7.0 mmol) in anhydrous dichloromethane (2.0 ml) and a 1% solution of Metatin 712 in dichloromethane (2.0 ml) were added and the reaction mixture was stirred for 15 h at room temperature. After concentrating in vacuo the obtained crude product was purified by column chromatography (eluent: ethyl acetate/methanol 95:5). 3.85 g (90% yield) of the product was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040602B2
Source datasetuspto-grants-2015_05
ORD IDord-31090dd04dc34820b2964d556adf61e7
Source noteuspto-grants-2015_05