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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662055Generated: October 30, 2026

Dimethylformamide → Ethyl 3-[(tert-butoxycarbonyl)(2-methoxyethyl)amino]benzoate

https://huagongshe.com/reaction/1662055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantEthyl 3-[(tert-butoxycarbonyl)amino]benzoateHCID 22643546—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-[(tert-butoxycarbonyl)(2-methoxyethyl)amino]benzoateHCID 5945398758.3%

Reaction Steps

To a mixture of ethyl 3-[(tert-butoxycarbonyl)amino]benzoate (3.8 g) and DMF (20 ml) were added 60% sodium hydride (1.1 g) and 2-bromoethylmethyl ether (3.9 g) under ice-cooling, followed by stirring at room temperature over one night. To the reaction mixture were added 60% sodium hydride (0.28 g) and 2-bromoethylmethyl ether (0.98 g), followed by stirring at room temperature for 6 hours. Water and ethyl acetate were added thereto, and the organic layer was then separated, washed with 1 M hydrochloric acid and saturated brine in this order, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain ethyl 3-[(tert-butoxycarbonyl)(2-methoxyethyl)amino]benzoate (2.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030489B2
Source datasetuspto-grants-2011_10
ORD IDord-838617da2740488885246466c41f38ed
Source noteuspto-grants-2011_10