HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86752572, compound → HCID 86752571, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86752572 | HCID 86752572 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86752571 | HCID 86752571 | — |
Reaction Steps
To a solution of dihydro-3-bromo-1-pyrindine-6,6-diphosphonic acid tetraethylester (10 mmol) in THF (10 ml) cooled to -78° C. is added a solution of n-butyllithium (2.1 equiv) in hexane over 30 minutes. The reaction is kept at -78° C. for an additional 30 minutes. To this solution is added 2-iodoethanol trimethylsilyl (TMS) ether (2.5 equiv) and the reaction is allowed to warm to room temperature over 30 minutes. After standard aqueous work-up, dihydro-3-(2-hydroxyethanol, TMS ether)-1-pyrindine-6,6-diphosphonic acid tetraethyl ester is isolated and used in the subsequent reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753634 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-47129dd772464b70a3822a209141e8b9 |
| Source note | uspto-grants-1998_05 |