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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440963Generated: November 2, 2026

Methyl chloroformate → Methyl 2-(4,6-dimethoxypyrimidin-2-yl)-2-fluoro-2-phenylacetate

https://huagongshe.com/reaction/1440963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
Reactant4,6-Dimethoxy-2-(alpha-fluorobenzyl) pyrimidineHCID 54101218—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(4,6-dimethoxypyrimidin-2-yl)-2-fluoro-2-phenylacetateHCID 22420764—

Reaction Steps

n-Butyllithium (2.5M in hexane, 1.7 ml) was added to diisopropylamine (0.59 ml) under nitrogen in dry tetrahydrofuran (15 ml) at -78° C. This solution was stirred for 30 minutes, then a solution of the product of stage (a) above (1.0 g) in tetrahydrofuran (10 ml) was added over 20 minutes. Methyl chloroformate (0.4 g) in dry tetrahydrofuran (10 ml) was added over 15 minutes at -78° C., and the reaction mixture was allowed to warm slowly to room temperature, after which it was added to aqueous ammonium chloride solution. The mixture was extracted with ether, the extracts being washed with water, dried over magnesium sulfate, and evaporated to dryness to give 1.08 g of the desired product, identical to that of Method A above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05502028
Source datasetuspto-grants-1996_03
ORD IDord-1b7bd2fdfe634330967fe57bb3cd7801
Source noteuspto-grants-1996_03