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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507719Generated: November 4, 2026

Phenethyl bromide → HCID 19026043, compound

https://huagongshe.com/reaction/507719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantHCID 11604517HCID 11604517—
ProductHCID 19026043HCID 19026043184.8%

Reaction Steps

436.4 g (1.0 mol) of 3,9-di(2-phenylethoxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5,5]undecane and 370.1 g (2.0 mol) of 2-phenylethyl bromide were charged into a reactor equipped with a stirrer, thermometer and capacitor, and dry nitrogen was caused to flow into the reactor under agitation at room temperature. Thereafter, heating was started with an oil bath which was kept at 180° C. for 10 hours. The oil bath was removed to cool the reactor to room temperature. 2,000 ml of methanol was added to the obtained reaction product which was a white solid and stirred to clean the reaction product, and the white powder was separated by filtration with a glass filter. Then, the separated white powder was cleaned with 2,000 ml of a 50 wt % aqueous solution of methanol and dried at 100 Pa and 120° C. for 8 hours to produce 362.3 g of 2,4,8,10-tetraoxa-3,9-diphosphaspiro[5,5]undecane, 3,9-di (2-phenylethyl)-3,9-dioxide. It was confirmed from mass spectral analysis, 1H, 31P nuclear magnetic resonance spectral analysis and elemental analysis that the product was bis-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5,5]undecane, 3,9-di(2-phenylethyl)-3,9-dioxide. This compound had a yield of 83%, an HPLC purity of 99.3% and an acid value of 0.41 mgKOH/g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786197B2
Source datasetuspto-grants-2010_08
ORD IDord-71f1dbebcaf94be19a4c5475d811c29a
Source noteuspto-grants-2010_08