HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 378512Erstellt: 24. Oktober 2026
Acetone → N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine
https://huagongshe.com/de/reaction/378512
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetone | HCID 180 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 5-(4-Bromomethylphenyl)-2-methyl-2H-tetrazole | HCID 589329 | — |
| Edukt | 4-[Bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine | HCID 19040926 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine | HCID 15515185 | 32,9% |
Reaktionsschritte
This compound was prepared in a manner analogous to that of Step D of Example 4, with 0.3 gram (0.001 mole) of 4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl bromide, 0.5 gram (0.001 mole) of 4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine (prepared as in Step C of Example 4), and 0.6 gram (0.004 mole) of N, N-diisopropylethylamine in about 5 mL of dimethyl sulfoxide as reagents. The crude reaction product was subjected to column chromatography on silica gel, with 3:7 acetone:methylene chloride as the eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding about 0.2 gram of N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine. The NMR spectrum was consistent with the proposed structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06030987 |
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| Quelldatensatz | uspto-grants-2000_02 |
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| ORD ID | ord-bcb5a56cc3a54c96b180134c7064c21f |
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| Quellennotiz | uspto-grants-2000_02 |
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