HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 18461547, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | hexahydro-2H-cyclopenta[b]furan-2-one | HCID 11665410 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18461547 | HCID 18461547 | — |
Reaction Steps
Analogously to the procedure of Example 1, the title compound is was prepared from 1.2 g (9.5 nmuol) of hexahydro-cyclopenta[b]furan-2-one, 10 ml of 1 molar lithium bis-(trimethylsilyl)-amide solution in THF and 1.29 g (9.5 mmol) of allyl bromide in 20 ml of THF. Yield: 1.25 g (79%) of a colourless oil. 1H-NMR(200 MHz; [d6]-DMSO): δ[ppm]: 1.47-1.89 (br m,6H), 2.15-2.55 (br m,4H), 4.41 (m,1H), 5.12 (dd,1H), 5.18 (dd,1H), 5.76 (ddt,1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06433004B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-dc5ebddfb923426c8b77fcefa126918e |
| Source note | uspto-grants-2002_08 |