HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370286Generated: October 30, 2026
Hydrochloric Acid → HCID 70237563, compound
https://huagongshe.com/reaction/370286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 21188359 | HCID 21188359 | — |
| Product | HCID 70237563 | HCID 70237563 | 97.3% |
Reaction Steps
2 g (0.0066 mol) of tert-butyl 4-(2-methoxycarbonylmethoxyethyl)piperazine-1-carboxylate prepared in Example I.4.3. are dissolved in 10 ml of ethanol in a 50 ml three-necked round-bottomed flask fitted with a water-cooled condenser and a mechanical stirrer. 11 ml of a 3.8M solution of hydrochloric acid in ethanol are added in a single portion with stirring. The mixture is stirred at room temperature for 30 minutes and a further 11 ml of a 3.8M solution of hydrochloric acid in ethanol are added. The mixture is brought at the reflux temperature for 4 hours. The solvent is removed on a rotary evaporator under reduced pressure. 1.86 g (97.3%) of ethyl 2-(1-piperazinyl)-ethoxyacetate dihydrochloride are obtained in the form of a pale yellow oil which crystallizes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06140501 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-8645fc4fc7674ba991623b5380c465ba |
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| Source note | uspto-grants-2000_10 |
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