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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247634Generated: October 31, 2026

Phosphorus oxychloride → (+/-)-2,4-Dichloro-5-(1-chloroethyl)-pyrimidine

https://huagongshe.com/reaction/1247634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(2,4-Dichloropyrimidin-5-yl)ethan-1-olHCID 15141648—
SolventTolueneHCID 1140—
Product(+/-)-2,4-Dichloro-5-(1-chloroethyl)-pyrimidineHCID 21908976—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (±)-1-(2,4-dichloro-pyrimidin-5-yl)-ethanol (1.27 g, 6.60 mmol) (from Example 1a supra) in phosphorus oxychloride (5.0 mL, 53.11 mmol) (Aldrich), at 0° C., was added diisopropylethyl-amine (2.60 mL, 14.78 mmol) (Aldrich). The reaction was stirred at 0° C. for 5 minutes, at ambient temperature for 15 minutes and then at 115° C. for 3 hours. The reaction was cooled to room temperature, diluted with toluene (10 mL) and the mixture was then poured into ice (15 g). After stirring for 10 minutes, the layers were separated and the aqueous extract was back washed with toluene. The combined organic extracts were dried over anhydrous sodium sulfate, filtered, and concentrated. Purification by flash chromatography (Biotage, 40M, 10:90 to 15:85 ethyl acetate-hexanes gradient) gave (±)-2,4-dichloro-5-(1-chloroethyl)-pyrimidine as an oil. (Yield 1.233 g; 88.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129351B2
Source datasetuspto-grants-2006_10
ORD IDord-ed9ec06b2bbe43fa9cdfbd2e97309a22
Source noteuspto-grants-2006_10