Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368811Generated: November 2, 2026

Potassium Bromide → HCID 66580034, compound

https://huagongshe.com/reaction/2368811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantSodium BicarbonateHCID 516892—
ReactantTempoHCID 2724126—
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 66580196HCID 66580196—
CatalystTempoHCID 2724126—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66580034HCID 6658003495%

Reaction Steps

To a solution of 8-hydroxy-2-[4-((R)-2,2,2-trifluoro-1-methyl-ethoxy)-phenyl]-2-aza-spiro[4.5]decan-1-one (5.79 g) and 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO) (506 mg) in CH2Cl2 (85 ml) was added a solution of potassium bromide (482 mg) in water (16 mL). Then, sodiumhypochlorite (13%, 42.5 mL) was added dropwise over a period of 10 minutes followed by sodium bicarbonate (NaHCO3) (4.08 g). The mixture was stirred for 1.5 h at RT. TLC showed a remainder of starting material. More TEMPO (125 mg) and sodiumhypochlorite solution (10 mL) were added to the reaction mixture and the mixture was stirred for additional 2 h at RT. The reaction mixture was poured into ice/water and was extracted three times with CH2Cl2. The combined organic layers were washed with brine, dried over Na2SO4, filtered and the solvent was evaporated. The crude material was purified by flash chromatography (silica gel, gradient of heptane in ethyl acetate) to provide the title compound as a light brown solid (5.47 g). MS (m/e): 356.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703807B2
Source datasetuspto-grants-2014_04
ORD IDord-fe7c3af33c7e47a2abf2161f01bdc1eb
Source noteuspto-grants-2014_04