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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603948Generated: November 1, 2026

Ethyl bromoacetate → Ethyl 4-(1,1-dimethylethoxycarbonyl)amino-3-methylphenoxyacetate

https://huagongshe.com/reaction/1603948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantCesium carbonateHCID 10796—
Reactanttert-Butyl (4-hydroxy-2-methylphenyl)carbamateHCID 15429162—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-(1,1-dimethylethoxycarbonyl)amino-3-methylphenoxyacetateHCID 1542916878%

Reaction Steps

To a 200 mL round bottomed flask with a stirring bar, and an argon inlet was added 4-(1,1-dimethylethoxycarbonyl)amino-3-methylphenol (5.00 g, 22.39 mmol), Cs2CO3 (14.59 g, 44.78 mmol), DMF (50 mL), and ethyl bromoacetate (2.61 mL, 23.51 mmol). This mixture was stirred vigorously at ambient temperature for 24 h. The mixture was filtered through a frit and the DMF was removed under high vacuum. The residue was dissolved in EtOAc (300 mL) and washed with H2O (2×) and brine (1×). Drying (MgSO4), filtration, and removal of the solvent in vacuo gave a solid. This material was triturated with 5% Et2O-hexane, the solid was collected by filtration and dried in vacuo to give 5.40 g (78%) of ethyl 4-(1,1-dimethylethoxycarbonyl)amino-3-methylphenoxyacetate as a white, crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990107
Source datasetuspto-grants-1999_11
ORD IDord-f57feb17cd954b09aab2cf1344af6e32
Source noteuspto-grants-1999_11