HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110145Generated: October 30, 2026
p-(Trifluoromethoxy)benzaldehyde → HCID 57565304, compound
https://huagongshe.com/reaction/2110145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-(Trifluoromethoxy)benzaldehyde | HCID 69573 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | rel-(2R,6S)-2,6-dimethylpiperazine | HCID 6950261 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57565304 | HCID 57565304 | 80% |
Reaction Steps
To a solution of 4-(trifluoromethoxy)-benzaldehyde (776 uL, 4.38 mmol) in methylene chloride (30 mL) was added cis-2,6-dimethyl piperazine (1.0 g, 8.77 mmol). After 1 hour sodium triacetoxy borohydride (2.45 g, 8.77 mmol) was added to the mixture. The solution was stirred at room temperature for an additional 4 hours. The reaction was concentrated in vacuo, diluted with ethyl acetate and extracted with 1N HCl (2×50 mL). The aqueous layer was then neutralized with NaOH and extracted with ethyl acetate (3×50 mL). The organic layer was dried (Na2SO4) and concentrated to provide cis-3,5-dimethyl-1-(4-trifluoromethoxy-benzyl)-piperazine (1.01 g, 80%). 1H NMR (400 MHz, CD3OD) δ 7.42 (d, 2H), 7.23 (d, 2H), 3.54 (s, 2H), 2.98-2.88 (m, 2H), 2.82-2.74 (m, 2H), 1.69 (t, 2H), 1.05 (d, 6H); LCMS 289.5 (M+I)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517884B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-e31ccce69abf400b927ec9c2cbf0914a |
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| Source note | uspto-grants-2009_04 |
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