HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86749086, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 15297251 | HCID 15297251 | — |
| Reactant | HCID 86749088 | HCID 86749088 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 86749086 | HCID 86749086 | 84% |
Reaction Steps
Allyl 6β-[(1,3-dithiolan-2-ylidene)(methoxycarbonyl)acetamido]-2,2-dimethylpenam-3-carboxylate (459 mg, 1 mmol) was dissolved in 0.25N sodium 2-ethylhexanoate/ethyl acetate solution (4 mL), and treated with triphenylphosphine (30 mg) and tetrakis(triphenylphosphine)palladium(0) (30 mg). The reaction mixture was stirred at room temperature for 2 h under a nitrogen atmosphere. The resulting precipitate was collected by filtration, washed with ethyl acetate and diethyl ether, and dried in vacuo to yield the title compound (368 mg, 84%) as a light yellow powder: 1H NMR (D2O) δ 1.40 and 1.50 (each 3H, s, C2 -(CH3)2), 3.25-3.45 (4H, m, SCH2CH2S), 3.69 (3H, s, OCH3), 4.13 (1H, s, C3 -H), 5.45-5.52 (2H, m, C5 -H and C6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05464616 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-677d17838aaf4f04bd3bc86545bcc9c0 |
| Source note | uspto-grants-1995_11 |