HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → (2S)-2-(Diphenylmethyl)oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | (2S)-3,3-diphenyl-propane-1,2-diol | HCID 54762284 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (2S)-2-(Diphenylmethyl)oxirane | HCID 11816639 | 77.5% |
Reaction Steps
A solution of (2S)-3,3-diphenyl-propane-1,2-diol (3.5 g, 15.35 mmol), Ph3P (8.05 g, 30.7 mmol), and DEAD (5.4 g, 30.7 mmol) in benzene (50 ml) was refluxed for 24 h. Solvent was removed and the residue was diluted with ethyl ether (200 ml) to precipitate Ph2PO. The filtrate was concentrated and the residue was chromatographed on silica gel (hexane/ether=9:1) to give (2S)-2-benzhydryl-oxirane 23b 2.5 g (78%, ([α]D=(−)9.6, c=1, MeOH). The 1HNMR and 13CNMR were identical with (R)-isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841464B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-1cdf6805acd84de2ab43cd3648b16dfd |
| Source note | uspto-grants-2014_09 |