HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174514Generated: October 27, 2026
Heptane → [4-(4-Methylpiperazine-1-carbonyl)phenyl]methanol
https://huagongshe.com/reaction/1174514
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Methyl 4-(hydroxymethyl)benzoate | HCID 81325 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [4-(4-Methylpiperazine-1-carbonyl)phenyl]methanol | HCID 59557836 | — |
Reaction Steps
To a solution of N-methyl piperazine (3.33 ml, 30.09 mmol) was added a solution of trimethylaluminium in heptane (15.04 ml, 30.09 mmol) and the mixture was stirred 10 min at room temperature. To this solution was added a solution of 4-(hydroxymethyl)benzoic acid methyl ester (1000 mg, 6.02 mmol) in DCE and the mixture was refluxed under inert atmosphere for 3 h. The mixture was diluted with DCM then water was added. The suspension was filtered through celite. The filtrate was washed with a solution 5% of NaHCO3 (2×) then water and brine. The organic layers were dried over MgSO4, evaporated and dried at 40° C. under vacuum to afford 307 mg (Y=21%) of the title compound as an oil. 1H NMR (DMSO-d6) δ 7.45-7.37 (m, 4H), 5.33 (t, J=5.6 Hz, 1H), 4.58 (br d, 2H), 3.77-3.50 (m, 4H), 2.46-2.30 (m, 4H), 2.26 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838522B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-285d4dda2a024ce9a6fd5ad7c467ef4d |
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| Source note | uspto-grants-2010_11 |
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