HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906165Generated: November 1, 2026
Lithium hydroxide, monohydrate → HCID 23702578, compound
https://huagongshe.com/reaction/1906165
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Ethyl 1-propylpiperidine-3-carboxylate | HCID 13905178 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23702578 | HCID 23702578 | — |
Reaction Steps
Ethyl N-propylnipecotate (73.86 g) was dissolved in 500 ml ethanol, treated with lithium hydroxide monohydrate (15.57 g) at reflux for 24 hours. Upon evaporation and drying in vacuo (100° C., eight hours), lithium N-propylnipecotate was obtained (white powder; 60 g). A solution of 17.7 g of this salt in 200 ml THF was treated dropwise with one equivalent of methyl-lithium, at 0° C. After stirring at room temperature overnight, an aqueous work-up yielded 3-acetyl-N-propylpiperidine (mp of HCl salt 108°-111° C.). When 2.5 of this compound were intimately mixed with 2.28 g of thiourea and 3.81 g of iodine and heated on a steam bath for 24 hours, followed by a column chromatography (Silica; acetone) and salt formation by the procedure of Example 2, 1.75 g of 4-(1-propyl-3-piperidyl)-2-thiazolamine hydrochloride (mp 243°-248° C.) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04650805 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-ff35f3dfe4554896b88902221a640173 |
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| Source note | uspto-grants-1987_03 |
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