HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403549Generated: October 29, 2026
Hydrochloric Acid → HCID 131731754, compound
https://huagongshe.com/reaction/2403549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 24781220 | HCID 24781220 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131731754 | HCID 131731754 | 14% |
Reaction Steps
A solution of 0.77 mL (1.3 mmol) of potassium tert-pentoxyde solution (1.7M in toluene) is added dropwise at room temperature to a stirred solution of 52 mg (1.27 mmol) of acetonitrile in 2.5 mL of tetrahydrofuran followed by dropwise addition of 0.19 g (0.44 mmol) of (4-{2-[4-(3-trifluoromethylphenyl)piperazin-1-yl]ethyl}piperidin-1-yl)acetic acid ethyl ester in 1 mL of tetrahydrofuran. After 30 minutes at room temperature, the reaction mixture is diluted with 10 mL of an aqueous 0.2N aqueous hydrochloric acid solution and 50 mL of ethyl acetate forming an emulsion. The mixture is concentrated under reduced pressure and the product is purified over 10 g of silica gel (eluant dichloromethane/methanol 95/5). The oily product is dissolved in 2 mL of diethyl ether and acidified with a hydrochloric acid diethyl ether solution. The precipitate is filtered, washed with diethyl ether and dried under reduced pressure to give 30 mg (14%) of 3-oxo-4-(4-{2[4-(3-trifluoromethylphenyl)piperazin-1-yl]ethyl}piperidin-1-yl)butanenitrile, dihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802678B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-7b89de86502e4c67af8121e2c2e96b60 |
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| Source note | uspto-grants-2014_08 |
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