HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-BUTYL CHLORIDE → 1-Adamantyl tert-butyl phosphine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-BUTYL CHLORIDE | HCID 10486 | — |
| Reactant | 1-Adamantylphosphine | HCID 11768954 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Adamantyl tert-butyl phosphine | HCID 68407015 | — |
Reaction Steps
nBuLi (20 cm3, 32 mmol 1.6M soln) was added over 1 hour to a cooled solution of 1-adamantyl phosphine (5.0 g, 30 mmol) in THF (100 cm3). The solution was allowed to warm to room temperature and stirred for a further 2 hours. The solution was recooled to 0° C. and tert-butylchloride (2.78 g, 30 mmol) was added and stirring continued for a further 16 hours at room temperature. The reaction mixture was quenched with water and the aqueous phase extracted with dichloromethane (2×50 ml). The organic phase was dried over sodium sulphate and evaporated in-vacuo to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07485739B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-dd3afb9a22d44d6a9990e8eb325cf9de |
| Source note | uspto-grants-2009_02 |