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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577555Generated: October 31, 2026

N-bromobutanimide → Ethyl 3-bromo-2-hydroxy-6-methyl-5-((methylsulfonyl)oxy)benzoate

https://huagongshe.com/reaction/577555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 86723781HCID 86723781—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-bromo-2-hydroxy-6-methyl-5-((methylsulfonyl)oxy)benzoateHCID 8672378279%

Reaction Steps

To a solution of ethyl 6-hydroxy-2-methyl-3-((methylsulfonyl)oxy)benzoate (116c, 1.3 g, 4.8 mmol) in acetonitrile (63 mL) was added N-bromosuccinimide (1.1 g, 6.2 mmol). The reaction was stirred at room temperature for 20 hours. The reaction mixture was concentrated under vacuum then diluted with water (30 mL) and extracted with dichloromethane (2×50 mL). The combined organic layers were washed with brine (30 mL), dried over magnesium sulfate, concentrated under vacuum, and purified by column chromatography (30% EtOAc/Heptane) to give ethyl 3-bromo-2-hydroxy-6-methyl-5-((methylsulfonyl)oxy)benzoate (116d, 1.3 g, 79% yield) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040515B2
Source datasetuspto-grants-2015_05
ORD IDord-412e725d5850438f96a6c40863d7a67e
Source noteuspto-grants-2015_05