HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53234Generated: October 30, 2026
Hydrochloric Acid → HCID 67714944, compound
https://huagongshe.com/reaction/53234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl oxalate | HCID 11120 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-Benzyl-4-Acetyl4-(4-Chlorobenzyl)-piperidine | HCID 19962174 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 67714944 | HCID 67714944 | 50.8% |
Reaction Steps
A solution of N-Benzyl-4-Acetyl-4-(4-Chlorobenzyl)-piperidine (600 mg, 1.75 mmol) and dimethyl oxalate (310 mg, 2.63 mmol) in dimethoxyethane (20 mL) was treated with sodium hydride (105 mg of a 60% dispersion in mineral oil, 2.63 mmol) and heated to reflux for 3 hours. The reaction was then cooled to room temperature, poured into 1 N aqueous HCl (200 mL) and extracted with ethyl ether (1×50 mL). The ether extract was discarded. The pH of the aqueous phase was adjusted to pH 8 and extracted with ethyl acetate (3×200 mL). The combined extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated at reduced pressure. The crude ester thus obtained was dissolved in THF (5 mL) and 3 N HCl (20 mL) and heated to reflux for 1 hour. The reaction was then cooled to room temperature, and concentrated at reduced pressure. The residue was triturated with tetrahydrofuran and the solid collected by filtration and crystallized from isopropanol to give 200 mg of the title compound. mp. 189°-181° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05618830 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-93cb5847f89c45208aab8d85dcdc66e3 |
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| Source note | uspto-grants-1997_04 |
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