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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13741Generated: October 29, 2026

Acetone → Dibutyl (2-hydroxypropan-2-yl)phosphonate

https://huagongshe.com/reaction/13741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
ReactantDibutylphosphiteHCID 23414612—
CatalystTriethylamineHCID 8471—
CatalystMagnesium ChlorideHCID 5360315—
ProductDibutyl (2-hydroxypropan-2-yl)phosphonateHCID 24027691.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

Next, into a two-liter four-necked flask provided with a stirrer, a thermometer, a dropping device, a hydrochloric-acid-recovering device and a condenser, 213.4 g (1.1 moles) of dibutyl phosphite, 5.6 g (0.06 moles) of triethylamine and 1.9 g (0.020 moles) of magnesium chloride were fed. While stirring the resulting mixed solution at 40° C., 70.2 g (1.2 moles) of acetone was added thereto in an hour. The mixed solution was further stirred for 1 hour at the same temperature (40° C.) to complete the reaction. Thereafter, the resulting reaction solution was washed with a 1% dilute hydrochloric acid aqueous solution and a saturated sodium carbonate aqueous solution successively and rinsed with water twice to remove the triethylamine and the magnesium chloride. Then, while heating the reaction mixture to 80° C., water was recovered under a reduced pressure of about 2.7 kPa. Further, nitrogen topping was carried out under the same conditions to remove the low-boiling point portions, thereby obtaining 254.6 g of dibutyl(1-hydroxy-1-methylethyl)phosphonate (raw material 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728162B2
Source datasetuspto-grants-2010_06
ORD IDord-0ea2bdc4c866408ab508898c07c300dd
Source noteuspto-grants-2010_06