HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272283Generated: October 31, 2026
Hydrochloric Acid → 1-(4-Methoxyphenyl)-4-(2,2,4,6,7-pentamethyl-3-methylidene-2,3-dihydro-1-benzofuran-5-yl)piperazine
https://huagongshe.com/reaction/1272283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-(2,2,3,4,6,7-Hexamethyl-3-hydroxy-2,3-dihydro-1-benzofuran-5-yl)-4-(4-methoxyphenyl)piperazine | HCID 22935608 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(4-Methoxyphenyl)-4-(2,2,4,6,7-pentamethyl-3-methylidene-2,3-dihydro-1-benzofuran-5-yl)piperazine | HCID 22935575 | 92.3% |
Reaction Steps
A solution of 10% hydrochloric acid (5 ml) was added to a solution of 1-(2,2,3,4,6,7-hexamethyl-3-hydroxy-2,3-dihydro-1-benzofuran-5-yl)-4-(4-methoxyphenyl)piperazine (1.70 g, 4.14 mmol) obtained in Reference Example 26 in acetonitrile (15 ml) at room temperature and the mixture was stirred for 6 hours. The resulting mixture was concentrated under reduced pressure, and the residue was made to basic with 10% aqueous potassium carbonate. The aqueous layer was extracted with ethyl acetate. The organic extract was washed with water and saturated aqueous sodium chloride, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure and the residue was crystallized from ethanol to obtain 1.50 g (yield 92%) of the title compound. mp. 134–136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208495B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-f16357ccae1d470687c2d1756f9a2d5c |
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| Source note | uspto-grants-2007_04 |
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