HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736325Generated: November 3, 2026
Phosphate → 2-(Dibenzyloxyphosphinyloxymethyl)-4-(3-methylbutyl)-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide
https://huagongshe.com/reaction/1736325
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Dibenzylphosphate | HCID 4193600 | — |
| Reactant | Cesium | HCID 5354618 | — |
| Reactant | HCID 15817425 | HCID 15817425 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Dibenzyloxyphosphinyloxymethyl)-4-(3-methylbutyl)-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide | HCID 9957989 | 15% |
Reaction Steps
To the cesium salt of dibenzyl phosphate (Formula III: A=B=CH2Ph) (prepared from 2.07 g of the phosphate and 1.21 g of cesium carbonate in methanol followed by removal of the methanol) in 30 ml of DMF was added 2-chloromethyl-4-(3-methylbutyl)-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (1 g; 3.72 mmol) and the mixture was allowed to stir at room temperature for 48 hours. The mixture was poured into ice/water, extracted with ethyl acetate, and the organic layer was washed with water, brine and dried. The solvent was concentrated in vacuo and the residue purified by silica gel flash chromatography (60% ethyl acetate/hexane) to afford 0.29 g (15%) of 2-(dibenzyloxyphosphinyloxymethyl)-4-(3-methylbutyl)-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (Formula I: R1 =H; R2 =(CH2)2CH(CH3)2 ; R3 =CH3 ; A=B=CH2Ph) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05541168 |
|---|
| Source dataset | uspto-grants-1996_07 |
|---|
| ORD ID | ord-80a7a94ab31c4136ac61727147e92318 |
|---|
| Source note | uspto-grants-1996_07 |
|---|