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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841952Generated: October 30, 2026

Diethyl methylthiomethylphosphonate → HCID 86757952, compound

https://huagongshe.com/reaction/841952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl methylthiomethylphosphonateHCID 520377—
ReactantHCID 22618004HCID 22618004—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86757952HCID 8675795266.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

30.7 ml of n-butyl lithium (1.63 M, n-hexane solution) was diluted with 35 ml of THF, and the diluted solution was cooled to −78° C. in an atmosphere of argon. Thereto was added a solution of 10.4 g of diethyl methylthiomethylphosphonate in 10 ml of THF, followed by stirring at −78° C. for 1 hour. Thereto was added dropwise a solution of 5 g of 5-n-butyl-7-chloropyrazolo[1,5-a]pyrimidine in 5 ml of THF, followed by stirring at −78° C. for 1 hour. The reaction mixture was diluted with ethyl acetate and washed sequentially with aqueous ammonium chloride solution, water and saturated saline and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent; ethyl acetate:n-hexane=1:3→1:1). As a result, 5.9 g of diethyl (5-n-butylpyrazolo[1,5-a]pyrimidin-7-yl)methylthiomethylphosphonate was obtained as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372749B1
Source datasetuspto-grants-2002_04
ORD IDord-f1760fb48a844112918265882e75dbe1
Source noteuspto-grants-2002_04