HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374802Generated: October 30, 2026
HCID 10202989, compound → HCID 68420335, compound
https://huagongshe.com/reaction/2374802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 10202989 | HCID 10202989 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68420335 | HCID 68420335 | — |
Reaction Steps
1.40 g (3.25 mmol) of t-butyl 2-[4-(5H-dibenzo[a,d][7]annulen-5-ylidene)-1-piperidinyl]-2-oxoethylcarbamate was dissolved in 20 ml of 1,4-dioxane. 12 ml of 4 N hydrochloric acid/1,4-dioxane solution was added to the obtained solution, and they were stirred overnight. After the neutralization with 4 N aqueous sodium hydroxide solution, the solvent was evaporated under reduced pressure. Saturated aqueous sodium chloride solution was added to the reaction mixture. After the extraction with ethyl acetate 3 times, the extract was dried over anhydrous sodium sulfate and then the solvent was evaporated under reduced pressure. 10 ml of a solution of ethyl acetate:hexane (1:2) and then 2 ml of 4 N hydrochloric acid/1,4-dioxane solution were added to the residue. The resultant precipitates were taken by the filtration, washed with a solution of ethyl acetate:hexane (1:2) and air-dried. After further drying under reduced pressure, the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462630B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-a6199737e85a4dfbb304f9bd4354efdb |
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| Source note | uspto-grants-2008_12 |
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