Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092682Generated: November 1, 2026

Potassium Bromide → HCID 66580194, compound

https://huagongshe.com/reaction/2092682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantSodium BicarbonateHCID 516892—
ReactantTempoHCID 2724126—
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 66580295HCID 66580295—
CatalystTempoHCID 2724126—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66580194HCID 6658019495%

Reaction Steps

To a solution of 8-hydroxy-2-[4-((S)-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 hours at RT. TLC showed a remainder of starting material. More TEMPO (125 mg) and sodiumhypochlorite solution (10 mL) were added and the mixture was stirred for an additional 2 hours at RT. The reaction was poured into ice/water and was extracted three times with CH2Cl2. The combined organic layers were washed with brine, dried over Na2SO4 and filtered. The solvent was evaporated and 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 numberUS08440710B2
Source datasetuspto-grants-2013_05
ORD IDord-a4697f2c8ebe4dd6b531e3a12c1f5a5c
Source noteuspto-grants-2013_05