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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920095Generated: November 1, 2026

Ethyl Bromide → HCID 86639861, compound

https://huagongshe.com/reaction/1920095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 86639862HCID 86639862—
SolventDimethylformamideHCID 6228—
ProductHCID 86639861HCID 86639861—

Reaction Conditions

Temperature0 °C

Reaction Steps

While being maintained at 0° C., KOH (0.13 g, 2.4 mmol) was added to a solution of the (S)—N-{{3-[3,5-difluoro-4-(7-hydroxydimono?-5-azaspiro[2,4]heptan-5-yl)phenyl]-2-oxo-5-oxazolidinyl}methyl}acetamide (0.8 g, 1.4 mmol) obtained in Example 3 in 10 mL of DMF, and then slowly droplets of ethyl bromide (0.4 mL, 5.6 mmol) were added with stirring for 3 hours. After the reaction terminated, the reaction mixture was poured into cold water and extracted with ethyl acetate. The organic phase was washed with water and brine and dehydrated over anhydrous magnesium sulfate. Purification through flash column chromatography (n-hexane/ethyl acetate=1:4) afforded the target compound in a white pure form (0.52 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168797B2
Source datasetuspto-grants-2012_05
ORD IDord-7cfb43ec44584a7cb75e1c7428cf5b31
Source noteuspto-grants-2012_05