HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406368Generated: October 29, 2026
Benzylethanolamine → HCID 66618867, compound
https://huagongshe.com/reaction/406368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylethanolamine | HCID 4348 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 4-(Trifluoromethyl)benzaldehyde | HCID 67996 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66618867 | HCID 66618867 | 46.6% |
Reaction Steps
4-(Trifluoromethyl)benzaldehyde (CAS #455-19-6, 2 g) and methanol (1 mL) were added to a solution of sodium bisulfite (1.33 g) in water (40 mL) at room temperature, and the mixture was stirred at room temperature for 10 minutes. Sodium cyanide (1.33 g) was added to the reaction solution, and the mixture was stirred at the same temperature for 40 minutes. N-Benzylethanolamine (1.83 g) and methanol (3 mL) were added to the reaction solution, and the mixture was stirred at the same temperature for 16 hours. The reaction solution was partitioned with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent:heptane:ethyl acetate=9:1→1:1) to obtain 1.79 g of the title compound. The property values of the compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754100B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-a9fdb9b86cbf43e2815ac6d1d2d667c2 |
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| Source note | uspto-grants-2014_06 |
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