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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459421Generated: October 31, 2026

Dimethylformamide → Ethyl 2-(4-{[(tert-butoxy)carbonyl]amino}phenoxy)acetate

https://huagongshe.com/reaction/1459421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl bromoacetateHCID 7748—
ReactantCesium carbonateHCID 10796—
ReactantN-Boc-4-hydroxyanilineHCID 2756771—
SolventChloroformHCID 6212—
ProductEthyl 2-(4-{[(tert-butoxy)carbonyl]amino}phenoxy)acetateHCID 54043329102.8%

Reaction Steps

To a 500 mL round bottomed flask with a stirring bar and an argon inlet was added 4-(1,1-dimethylethoxycarbonylamino)phenol (8.20 g, 39.19 mmol), Cs2CO3 (25.54 g, 78.38 mmol), DMF (75 mL), and ethyl bromoacetate (4.78 mL, 43.11 mmol). This heterogeneous mixture was stirred at ambient temperature for 3.5 h. The mixture was diluted with a little CHCl3 and filtered through a frit to remove the salts. The DMF was removed under high vacuum and the residue was suspended in 500 mL of EtOAc. This mixture was washed with H2O (3×), and brine. Drying (MgSO4), filtration and removal of the solvent in vacuo, gave an oil. This material was chromatographed on 400 g of silica gel using 20% EtOAc-hexane as eluant. There was obtained 11.9 g (100%) of ethyl (4-(1,1-dimethylethoxycarbonylamino)phenoxy)acetate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854245
Source datasetuspto-grants-1998_12
ORD IDord-6033d6da4ae74af690ac9f3eda8e2847
Source noteuspto-grants-1998_12