HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433155Generated: October 31, 2026
Triethylamine → N-[3-benzyloxy-4-(2-bromo-acetyl)phenyl]-acetamide
https://huagongshe.com/reaction/1433155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Diethylphosphite | HCID 3780918 | — |
| Reactant | N-[3-benzyloxy-4-(2,2-dibromo-acetyl)phenyl]-acetamide | HCID 85978776 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-benzyloxy-4-(2-bromo-acetyl)phenyl]-acetamide | HCID 85606679 | 118.9% |
Reaction Steps
A solution of diethylphosphite (12.6 μL, 13.5 mg, 97.6 μmol) and triethylamine (13.6 μL, 9.9 mg, 97.6 μmol) in THF (0.1 mL) was added to a stirred solution of N-[3-benzyloxy-4-(2,2-dibromo-acetyl)-phenyl]-acetamide (41 mg, 92.9 μmol) in THF (1.5 mL) at room temperature, and the reaction stirred for 2 hours. The mixture was poured into EtOAc (20 mL) and washed with water (20 mL) and brine (20 mL). The organic layer was dried (MgSO4) and the solvent removed in vacuo to give N-[3-benzyloxy-4-(2-bromo-acetyl)-phenyl]-acetamide (40 mg, >100%), which was seen by NMR to be contaminated with a diethylphosphite-derived contaminant. The material could be used successfully in the following steps without further purification. All analytical data was as reported above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612201B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-e93ff9415bc248818b994272a26f7c21 |
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| Source note | uspto-grants-2009_11 |
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