Tetrahydrofuran → (2r,5r)-2,5-Dimethyl-1-phenylphospholane

One equivalent of n-BuLi (8.9 ml, 1.6 M. solution in n-hexane) is added slowly to a solution of 1.57 g phenylphosphine (14.3 mmol) in 100 ml of THF at −78° C. This is then stirred for a further two hours at room temperature. After cooling again to −78° C., one equivalent of the cyclic sulfate 1 in 10 ml of THF is added via a cannula and the reaction is allowed to end by stirring at 25° C. for 3 hours. Before adding a further 1.2 eq. of n-BuLi (9.8 ml) via syringe, the mixture is cooled again, n-BuLi is added and stirring is continued overnight. For the work-up, the solvent was drawn off in vacuo and the residue taken up in 5 ml of water and extracted with 50 ml of methylene chloride. After the phase separation the solvent is removed and the residue is distilled in vacuo. An almost colourless syrup is obtained in a yield of 71% (1.95 g).

1. temperatureAfter cooling again to −78° C.
2. stirringby stirring at 25° C. for 3 hours
3. temperaturethe mixture is cooled again
4. stirringstirring
5. waitis continued overnight
6. extractionextracted with 50 ml of methylene chloride
7. customAfter the phase separation the solvent
8. customis removed
9. distillationthe residue is distilled in vacuo
10. customAn almost colourless syrup is obtained in a yield of 71% (1.95 g)

ORDレコード

ord-4bf501b20eed4fd0b113b21e5cc51d39

出典データセット

uspto-grants-2008_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07361786B2