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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | N-Boc-4-hydroxyaniline | HCID 2756771 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 2-(4-{[(tert-butoxy)carbonyl]amino}phenoxy)acetate | HCID 54043329 | 102.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05854245 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-6033d6da4ae74af690ac9f3eda8e2847 |
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| Source note | uspto-grants-1998_12 |
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