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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378512Generated: October 25, 2026

Acetone → N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine

https://huagongshe.com/reaction/378512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-(4-Bromomethylphenyl)-2-methyl-2H-tetrazoleHCID 589329—
Reactant4-[Bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidineHCID 19040926—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
ProductN-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidineHCID 1551518532.9%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030987
Source datasetuspto-grants-2000_02
ORD IDord-bcb5a56cc3a54c96b180134c7064c21f
Source noteuspto-grants-2000_02