HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → HCID 86751735, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 86751736 | HCID 86751736 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86751735 | HCID 86751735 | — |
Reaction Steps
200 g (0.38 mol) of benzyl (1S,4S,5S)-6-(3,4-dimethoxy-benzyl)-7-oxo-4-[[(1-imidazolyl)thiocarbonyl]oxy]-2,6-diazabicyclo[3.2.0]heptane-2-carboxylate were heated to 80° C. in 4.21 liters of toluene. A solution of 213 ml (0.8 mol) of tributyltin hydride and 6.9 g (0.04 mol) of AIBN in 320 ml of toluene were added dropwise thereto while stirring. After completion of the dropwise addition the mixture was stirred at this temperature for a further 45 minutes before the solvent was removed under reduced pressure. There remained behind a yellowish turbid oil which was chromatographed over 1100 g of silica gel (0.063-0.2 mm particle size with 1) ethyl acetate: hexane 1:10; 2) ethyl acetate: hexane 2:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05712268 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-39651c8431b54996a17a146e46d6daee |
| Source note | uspto-grants-1998_01 |