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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563875Generated: October 31, 2026

Hydrochloric Acid → HCID 18357338, compound

https://huagongshe.com/reaction/563875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
Reactant3,4-Dihydro-2-hydroxy-4-phenyl-2H-1-benzopyran-6-ethanolHCID 58003501—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventTolueneHCID 1140—
ProductHCID 18357338HCID 1835733861%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067594B2
Source datasetuspto-grants-2011_11
ORD IDord-732f3b33d03c4e66b04b4a31767e0a71
Source noteuspto-grants-2011_11