HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2087259Generated: October 26, 2026
Sodium triacetoxyborohydride → N-(3-{1-[4-(3,4-Difluorophenoxy)benzyl]-4-piperidinyl}-4-methylphenyl)-2-methylpropanamide
https://huagongshe.com/reaction/2087259
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-(3,4-Difluorophenoxy)benzaldehyde | HCID 10585741 | — |
| Reactant | 2-Methyl-N-[4-methyl-3-(4-piperidinyl)phenyl]propanamide | HCID 16757254 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | N-(3-{1-[4-(3,4-Difluorophenoxy)benzyl]-4-piperidinyl}-4-methylphenyl)-2-methylpropanamide | HCID 16756754 | 54.1% |
Reaction Steps
To a solution of 4-(3,4-Difluorophenoxy)benzaldehyde (41.0 mg, 0.170 mmol) and 2-methyl-N-[4-methyl-3-(4-piperidinyl)phenyl]propanamide (45.0 mg, 0.170 mmol) in 1,2-dichloroethane (5.00 mL) was added sodium triacetoxyborohydride (110 mg, 0.520 mmol) and ACOH (10.0 μL, 0.170 mmol) at room temperature. The mixture was stirred overnight. The reaction mixture was quenched by saturated NaHCO3 solution (10 mL) and extracted with CH2Cl2 (3×10 mL). The combined organic layers were washed with brine, dried over MgSO4, concentrated in vacuo. The crude product was purified by preparative TLC using 5% NH3 (2.0 M in MeOH) in CH2Cl2 to give the desired product N-(3-{1-[4-(3,4-difluorophenoxy)benzyl]-4-piperidinyl}-4-methylphenyl)-2-methylpropanamide (44.0 mg, 54.0%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06727264B1 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-7e82839ddbae4c108c2241697923a6c3 |
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| Source note | uspto-grants-2004_04 |
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