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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846537Generated: October 30, 2026

Diisopropylamine → HCID 53772531, compound

https://huagongshe.com/reaction/846537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantEthyl (2-methylphenyl)acetateHCID 96528—
Reactant4,6-Dimethoxy-2-(methylsulfonyl)pyrimidineHCID 838363—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53772531HCID 5377253160.1%

Reaction Conditions

Temperature-75 °C

Reaction Steps

n-Butyllithium (10 ml of 2N solution in pentane) was added dropwise to a stirred solution of di-isopropylamine (2.0 g) in dry tetrahydrofuran (40 ml) under nitrogen at -10° C. After stirring at this temperature for 15 minutes, the solution was cooled to -75° C., and a solution of ethyl (2-methylphenyl)acetate (3.56 g) in tetrahydrofuran (20 ml) was added dropwise. After stirring at -75° C. for one hour, 4,6-dimethoxy-2-(methylsulphonyl)pyrimidine (4.36 g) was added in one portion, and the resulting suspension was allowed to warm slowly to room temperature before stirring overnight. The reaction mixture was then poured onto water (400 ml) and the resulting oil was extracted into ether (2×150 ml). The combined extracts were washed with saturated sodium chloride solution, dried over magnesium sulphate and evaporated to give a yellow oil which was purified by chromatography to give 3.8 g of the desired product as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137564
Source datasetuspto-grants-1992_08
ORD IDord-992da6394fc242428a56b9f58eb0d7b4
Source noteuspto-grants-1992_08