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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803210Generated: November 1, 2026

N-bromobutanimide → 7-Bromo-9-(4-fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-on

https://huagongshe.com/reaction/1803210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant(9-(4-Fluorophenyl)-1,4-dioxaspiro[4.5]dec-7-en-8-yloxy)trimethylsilaneHCID 66858541—
SolventEthyl AcetateHCID 8857—
SolventOxolane--water (1/1)HCID 21881883—
Product7-Bromo-9-(4-fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-onHCID 58110113253%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349880B2
Source datasetuspto-grants-2013_01
ORD IDord-8f08471f7412444ead89459a4021daba
Source noteuspto-grants-2013_01