HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823903Generated: October 30, 2026
Potassium Carbonate → HCID 23570952, compound
https://huagongshe.com/reaction/1823903
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | Methyl 2-bromo-2-(3-methoxyphenyl)acetate | HCID 289522 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23570952 | HCID 23570952 | 53% |
Reaction Steps
To a solution of (3-methoxy-phenyl)-acetic acid methyl ester (19.6 mmol) in CCl4 was added N-bromosuccinimide (19.6 mmol) and the reaction mixture was irradiated for 2 hours. The reaction mixture was then concentrated in vacuo to afford the intermediate bromo-(3-methoxy-phenyl)-acetic acid methyl ester. To a solution of bromo-(3-methoxy-phenyl)-acetic acid methyl ester in THF (30 mL) under an atmosphere of nitrogen was added a solution of (2-amino-ethyl)-carbamic acid tert-butyl ester (20.6 mmol) in THF (20 mL) followed by K2CO3 (39.2 mmol, 2 equivalents). The reaction mixture was stirred for 2 hours at room temperature. The reaction mixture was partitioned between water (50 mL) and EtOAc (2×50 mL), the combined organics were dried (sodium sulfate) and concentrated in vacuo to afford an oil. The oil was purified by silica gel column chromatography using as eluent EtOAc:petrol (1:1) to give the title compound as an oil in 53% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07041687B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-ea60a30629e44818b8020be8cd25700e |
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| Source note | uspto-grants-2006_05 |
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