Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272385Generated: October 30, 2026

Phenylphosphonic dichloride → HCID 18456541, compound

https://huagongshe.com/reaction/1272385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylphosphonic dichlorideHCID 69990—
ReactantHCID 178517784HCID 178517784—
ProductHCID 18456541HCID 1845654166%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 669 mg (1.68 mmol) of 7,8-dibenzyl-2-(trifluoromethyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-ol and 1.2 mL of phenylphosphonic dichloride was heated in a sealed tube at 150° C. for 2.5 h. The mixture was cooled to ˜100° C., then poured into crushed ice, washing with ethyl acetate. The resultant biphasic mixture was neutralized with solid sodium bicarbonate to ˜pH 8 with vigorous stirring. The ethyl acetate layer was removed. The aqueous layer was extracted with ethyl acetate. The combined organic phases were washed sequentially with saturated aqueous sodium bicarbonate solution and brine, dried, and concentrated to give a red, viscous oil. Purification by Biotage chromatography (silica gel, 5% ethyl acetate/hexane) gave 464 mg (66%) of the title compound as a yellow solid. LC-MS 418.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208498B2
Source datasetuspto-grants-2007_04
ORD IDord-0b9b794e2cc0473d8ebe4de677fe2277
Source noteuspto-grants-2007_04