HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841952Generated: October 30, 2026
Diethyl methylthiomethylphosphonate → HCID 86757952, compound
https://huagongshe.com/reaction/841952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl methylthiomethylphosphonate | HCID 520377 | — |
| Reactant | HCID 22618004 | HCID 22618004 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86757952 | HCID 86757952 | 66.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06372749B1 |
|---|
| Source dataset | uspto-grants-2002_04 |
|---|
| ORD ID | ord-f1760fb48a844112918265882e75dbe1 |
|---|
| Source note | uspto-grants-2002_04 |
|---|