HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459412Generated: October 31, 2026
Ethyl bromoacetate → Ethyl 4-(1,1-dimethylethoxycarbonyl)amino-3-methylphenoxyacetate
https://huagongshe.com/reaction/1459412
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | tert-Butyl (4-hydroxy-2-methylphenyl)carbamate | HCID 15429162 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-(1,1-dimethylethoxycarbonyl)amino-3-methylphenoxyacetate | HCID 15429168 | 78% |
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% Et2 O-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
| 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-da8ae778ede6433caee061d1248faf80 |
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| Source note | uspto-grants-1998_12 |
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