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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330317Generated: October 31, 2026

Toluene → DL-5 Chloro-6-ethyl-4-[alpha-ethyl-4-(2,2-difluoropropoxy)benzyl]aminopyrimidine

https://huagongshe.com/reaction/330317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEthyl AcetateHCID 8857—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantDL-5 Chloro-6-ethyl-4-[alpha-ethyl-4-(1,1,2,2-tetrafluoroethoxy)benzyl]aminopyrimidineHCID 131716271—
SolventBenzeneHCID 241—
ProductDL-5 Chloro-6-ethyl-4-[alpha-ethyl-4-(2,2-difluoropropoxy)benzyl]aminopyrimidineHCID 13171627561.9%

Reaction Steps

To a solution of 1.0 g of dl-5-chloro-6-ethyl-4-(α-ethyl-4-acetonyloxybenzyl)aminopyrimidine obtained in Example 17 dissolved in 50 ml of dried benzene was added 0.5 g of diethylaminosulfur trifluoride, and the mixture was refluxed by heating for 5 hours while stirring. After completion of the reaction, the mixture was poured into ice-cold water and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The oily product obtained was isolated by column chromatography (Wako Gel C-200, trade name, eluted with toluene: ethyl acetate=7:1) to give 0.6 g of the desired product as pale yellow oily liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04895849
Source datasetuspto-grants-1990_01
ORD IDord-257f3afcb0c547779fb6655c55197a2a
Source noteuspto-grants-1990_01