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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778362Generated: November 1, 2026

Dimethylformamide → Tert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-(2-hydroxy-acetylamino)benzoate

https://huagongshe.com/reaction/1778362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-carbamoylmethoxybenzoateHCID 66685566—
ProductTert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-(2-hydroxy-acetylamino)benzoateHCID 66685058—

Reaction Steps

Sodium hydroxide (0.14 g) was added to a solution of tert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-carbamoylmethoxybenzoate (Intermediate 37, 0.33 g) in DMF (5 mL) and the mixture was stirred for 7 hours. Ethyl acetate and a saturated aqueous solution of sodium hydrogen carbonate were added to the mixture and the organic layer was separated, washed with water and brine, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and pentane with a gradient of 20-100%, to give tert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-(2-hydroxyacetylamino)-benzoate (0.17 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266896B2
Source datasetuspto-grants-2016_02
ORD IDord-cb59b3460a4e41fa9d553ada9ad01e8f
Source noteuspto-grants-2016_02