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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751914Generated: October 28, 2026

Potassium Bromide → HCID 59054016, compound

https://huagongshe.com/reaction/1751914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 24965836HCID 24965836—
SolventEthyl AcetateHCID 8857—
ProductHCID 59054016HCID 59054016—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To [4-(3,4-dichlorobenzyloxy)phenyl]-hydroxy-acetic acid methyl ester (750 g) in ethyl acetate (10 L) was added 2,2,6,6-tetramethylpiperidinyloxy (TEMPO) (10.15 g), KBr (26.25 g), and solid NaHCO3 (185.25 g) in a 22-liter round-bottom flask fitted with an overhead stirrer, thermocouple, and a dropping funnel. The reaction mixture was cooled to 0-5° C. using water/ice. To the cooled reaction mixture, bleach (3375 mL, CLOROX) was added dropwise at such a rate so as to maintain the internal temperature at 0-5° C. After addition of the bleach, the reaction mixture was allowed to reach room temperature and was stirred for 2 hours. LC-MS analysis showed that little of the starting material remained at this point. The reaction mixture was diluted with ethyl acetate (12 L) and the layers were separated. The aqueous layer was washed with ethyl acetate (4 L), and the two volumes of ethyl acetate were combined. The combined ethyl acetate layers were washed with water (10 L) and brine (10 L), dried over anhydrous sodium sulfate, concentrated, and filtered. The resulting solid was washed with hexanes (5 L) and dried at 40° C. under vacuum for 4 hours to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162963B2
Source datasetuspto-grants-2015_10
ORD IDord-86b758ac28cc45c7a9fbd16d3ede30ab
Source noteuspto-grants-2015_10