HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 7-Bromo-9-(4-fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-on
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (9-(4-Fluorophenyl)-1,4-dioxaspiro[4.5]dec-7-en-8-yloxy)trimethylsilane | HCID 66858541 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 7-Bromo-9-(4-fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-on | HCID 58110113 | 253% |
Reaction Steps
Step AAC (2): Followed a method described by A. de Meijer et. al Chem. Eur. J. 2007, 13, 3739. N-bromosuccinimide (52 mg, 0.29 mmol) was added to a solution of (9-(4-fluorophenyl)-1,4-dioxaspiro[4.5]dec-7-en-8-yloxy)trimethylsilane (89 mg, 276 mmol) in THF/water (1:1, 1.4 mL). The resulting mixture was allowed to stir for 2 hr. The crude reaction was diluted with EtOAc and washed with water. The organic layer was concentrated in vacuo to afford 7-bromo-9-(4-fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-on (230 mg, 253%) yield). The crude product was used for subsequent chemistry without purification or characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349880B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-8f08471f7412444ead89459a4021daba |
| Source note | uspto-grants-2013_01 |