Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 86760357 | HCID 86760357 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21072928 | HCID 21072928 | 131.8% |
Reaction Steps
A mixture of tert-butyl[3-(2-amino-5-chlorophenoxy)benzylcarbamate (5.2 g, 15 mmols), ethyl bromoacetate (3.3 ml, 30 mmols), potassium carbonate (2.1 g, 15 mmols) and N,N-dimethylformamide (30 ml) was stirred at 60° C. for 12 hours. The reaction mixture was cooled, poured into water, and extracted with ethyl acetate. The extract was washed with water, and then dried with anhydrous magnesium sulfate. This was concentrated under reduced pressure, and the residue was purified through silica gel column chromatography to give an oil of ethyl 2-[2-[3-(tert-butoxycarbonylaminomethyl)phenoxy]-4-chlorophenyl]aminoacetate (4.3 g, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160887B1 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-246aa91f89f74c39b156ba45ab619614 |
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| Source note | uspto-grants-2007_01 |
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