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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276390Generated: October 25, 2026

Sodium Acetate → 1,2-Benzenediol, 4-(3-hydroxypropyl)-

https://huagongshe.com/reaction/2276390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantOleuropeinHCID 5281544—
Product1,2-Benzenediol, 4-(3-hydroxypropyl)-HCID 11217464—
ProductOleuropein aglyconHCID 56842347—

Reaction Steps

Hydroxytyrosol was prepared from homogeneous oleuropein isolated from OLE. The procedure involves treatment of oleuropein with β-glycosidase (including but not limited to Sigma G4511) in 80 mM sodium acetate pH 5.0 using 1 Unit of enzyme/μ mole of substrate at 37° C. for 1 hr to remove the glucose moiety and to yield oleuropein aglycone. The oleuropein aglycone was then be treated with esterase (including but not limited to Sigma E0887) in sodium phosphate buffer at pH 7.5 using 1 Unit of enzyme/μ mole of substrate at 25° C. for 1 hr to yield hydroxytyrosol and elonelic acid. The final products were resolved and quantitated by LC-MS as described above. Detection and quantification were performed at 280 and 320 nm for hydroxytyrosol at 0.698 min (m/z 153) and oleuropein aglycone at 2.087 min (m/z 377). while 240 nm was used for the detection of elenolic acid at 1.846 min (m/z 241).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09132145B2
Source datasetuspto-grants-2015_09
ORD IDord-f2c2b42c0a8c441facce6bbfdbc14e41
Source noteuspto-grants-2015_09