HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563875Generated: October 31, 2026
Hydrochloric Acid → HCID 18357338, compound
https://huagongshe.com/reaction/563875
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 3,4-Dihydro-2-hydroxy-4-phenyl-2H-1-benzopyran-6-ethanol | HCID 58003501 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18357338 | HCID 18357338 | 61% |
Reaction Steps
A mixture of 6-(2-hydroxy-ethyl)-4-phenyl-chroman-2-ol (Example 7, 30 g, 111 mmol, 1 equiv), diisopropylamine (33.7 g, 333 mmol, 3 eq) and palladium hydroxide on carbon [50% wet catalyst (50% by weight is water), 6 g, 0.2 equiv] in toluene (120 mL) was hydrogenated at 621×103 Nm−2 (90 psi) hydrogen pressure at 110° C. The reaction mixture was cooled to room temperature and filtered through arbocel and evaporated under reduced pressure. The resulting oil was dissolved in acetonitrile (200 mL) and concentrated hydrochloric acid (11.6 mL, 1.05 equiv) was added. The mixture was distilled at ambient pressure, removing approximately 100 mL of acetonitrile, and the distilled solvent replaced with fresh acetonitrile. The mixture was allowed to cool and crystallise overnight. The product was filtered and washed with a small portion of acetonitrile and dried overnight in vacuo at 50° C. to give the title compounds as a white solid (26.7 g, 68.1 mmol, 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067594B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-732f3b33d03c4e66b04b4a31767e0a71 |
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| Source note | uspto-grants-2011_11 |
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