HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808347Generated: October 30, 2026
Benzylethanolamine → HCID 178499151, compound
https://huagongshe.com/reaction/1808347
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylethanolamine | HCID 4348 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Methyl 5-formyl-1H-imidazole-4-carboxylate | HCID 178499152 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178499151 | HCID 178499151 | 99% |
Reaction Steps
Methyl 4-formyl-1H-imidazole-5-carboxylate (1.68 mmol, 1 equiv.) was taken up in dry THF (10 ml). Dry Na2SO4 (15.53 mmol, 9.2 equiv.) and N-benzylethanolamine (1.99 mmol, 1.18 equiv.) were added, and the mixture was stirred for 1 h at 25° C. under nitrogen. NaBH(OAc)3 (2.36 mmol, 1.4 equiv.) was then added in portions, and the reaction mixture was stirred for 16 h. Then water (5 ml) was added, and the mixture was neutralised with sat. NaHCO3 solution (10 ml). Extraction with DCM (2×20 ml) was carried out, and the combined organic phases were dried over Na2SO4, filtered and concentrated in vacuo. The resulting crude product was purified by column chromatography (silica gel, 5-10% MeOH in DCM), and the desired product was thus obtained in the form of a white solid. Yield: 99%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357717B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-2199dc5a437048fbab7dbe0aa070d566 |
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| Source note | uspto-grants-2013_01 |
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