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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278581Generated: October 31, 2026

Ethyl Acetate → Ethyl 2-(4-chloro-6-methoxypyrimidin-2-yl)acetate

https://huagongshe.com/reaction/2278581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2,4-Dichloro-6-methoxypyrimidineHCID 3824509—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(4-chloro-6-methoxypyrimidin-2-yl)acetateHCID 86699270—

Reaction Conditions

Temperature-75 °C

Reaction Steps

91.4 ml of 1M lithium bis(trimethylsilyl)amide (THF) are added dropwise to a solution of 7.4 g of 2,4-dichloro-6-methoxypyrimidine and 4.5 ml of ethyl acetate in 100 ml of anhydrous THF cooled to −75° C. in a dry ice/acetone bath. The reaction medium is stirred at −75° C. for one hour. The cooling bath is removed so as to allow the temperature to rise to 22° C. The reaction medium is stirred at 22° C. for one hour. 100 ml of water and 400 ml of ethyl acetate are added. After settling out, the organic phase is dried over magnesium sulfate, filtered, and then concentrated under reduced pressure so as to give 9.5 g of (4-chloro-6-methoxypyrimidin-2-yl)acetic acid ethyl ester in the form of an orange oil, the characteristics of which are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133168B2
Source datasetuspto-grants-2015_09
ORD IDord-9f2c058dfccb480a84a97f2c9a65b736
Source noteuspto-grants-2015_09