HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776015Generated: October 30, 2026
Water → tert-Butyl 4-(4-(ethoxycarbonyl)phenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/1776015
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzoic acid, 4-fluoro-, ethyl ester | HCID 67976 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | tert-Butyl 4-(4-(ethoxycarbonyl)phenyl)piperazine-1-carboxylate | HCID 11709764 | 60% |
Reaction Steps
A mixture of piperazine-1-carboxylic acid tert-butyl ester (18.6 g, 0.1 mol), 4-fluoro-benzoic acid ethyl ester (16.8 g, 1 mol) and potassium carbonate (0.15 mol) in dimethylsulfoxide (100 mL) was stirred at 120° C. for 24 h. The reaction mixture was cooled to room temperature and poured into water (1 L). The solid precipitate was filtered, washed with water, and concentrated to dryness to provide the title compound (20 g, 60% yield) as a white solid. 1H NMR (CDCl3, 400 MHz) δ (ppm) 7.91 (d, 2H), 6.83 (d, 2H), 4.30 (q, 2H), 3.55 (m, 4H), 3.26 (m, 4H), 1.46 (s, 9H), 1.32 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260414B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-c8e6f44236794fd29a5e7be2655e679c |
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| Source note | uspto-grants-2016_02 |
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