HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608494Generated: October 31, 2026
Bromotrimethylsilane → HCID 86748521, compound
https://huagongshe.com/reaction/1608494
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | HCID 86748522 | HCID 86748522 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86748521 | HCID 86748521 | — |
Reaction Steps
1.5 g (2.4 mmol) of tetraethyl 2-[(3-methylsulfonyl-4-piperidylbenzoyl)-(aminoiminomethyl)amino]ethane-1,1-bisphosphonate from Example 1 are dissolved in 60 ml of absolute dioxane at 60° C. The reaction mixture is subsequently allowed to reach room temperature, and 1.64 g (10.8 mmol) of bromotrimethylsilane are added. The mixture is stirred at room temperature for 16 hours and subsequently heated at 60° C. for a further 4 hours. Solvent and volatiles are subsequently removed at 40° C./0.1 torr. 15 ml of water are then added to the residue, and the mixture is stirred at room temperature for 4 hours. The resulting residue is filtered off and washed several times with ethanol. The residue resulting from this is subsequently boiled in 20 ml of methanol and 10 ml of water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05395826 |
|---|
| Source dataset | uspto-grants-1995_03 |
|---|
| ORD ID | ord-e03f4ce3ff3b4b05a5e02525e7bb9c50 |
|---|
| Source note | uspto-grants-1995_03 |
|---|