HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972209Generated: October 30, 2026
4-Methoxybenzaldehyde → HCID 68703214, compound
https://huagongshe.com/reaction/1972209
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 28168138 | HCID 28168138 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68703214 | HCID 68703214 | — |
Reaction Steps
Crude (S)-[2-amino-1-(3-trifluoromethyl-phenyl)-ethyl]-carbamic acid ethyl ester from above is dissolved in anhydrous EtOH (100 mL). p-Anisaldehyde (2.07 g, 15.2 mmol) is added into the solution and stirred at room temperature for 5 h before the addition of NaBH4 (0.82 g, 21.8 mmol) at 0° C. The mixture is then warmed up to room temperature and stirred for 14 hr. After the solvent is removed under vacuum, the residue is treated with saturated NH4Cl aqueous solution (50 mL) and extracted with EtOAc (3×150 mL). The combined organic layer is washed with brine and dried (MgSO4). After removing the drying agent, the solution is concentrated to provide the crude (S)-[2-(4-methoxy-benzylamino)-1-(3-trifluoromethyl-phenyl)-ethyl]-carbamic acid ethyl ester as colorless oil (˜6.0 g) which is used directly for next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431607B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-d2ec52d72668465eb4aa2f8011748161 |
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| Source note | uspto-grants-2013_04 |
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