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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115923Generated: November 1, 2026

Potassium Carbonate → (+/-)-3-[2-(Benzyloxy)-3-tert-butylphenyl]propane-1,2-diol

https://huagongshe.com/reaction/2115923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Allyl-2-(benzyloxy)-3-tert-butylbenzeneHCID 68964286—
Reactant2-Methylpropan-2-ol--water (1/1)HCID 71401949—
Catalyst1,4-Bis((R)-((1S,2R,4S,5S)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methoxy)anthracene-9,10-dioneHCID 71311398—
CatalystHCID 178511488HCID 178511488—
Solventtert-ButanolHCID 6386—
Product(+/-)-3-[2-(Benzyloxy)-3-tert-butylphenyl]propane-1,2-diolHCID 6896642692%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of potassium ferricyanide (57.00 g, 0.173 mol), potassium carbonate (24.00 g, 0.174 mol), hydroquinine anthraquinone-1,4-diyl diether (0.495 g, 0.578 mmol), and potassium osmate dihydrate (0.043 g, 0.117 mmol) in water:tert-butyl alcohol (1:1, 600 mL) cooled to 0° C. was slowly added via an addition funnel a solution of 1-allyl-2-(benzyloxy)-3-tert-butylbenzene (16.2 g, 0.058 mol) in tert-butyl alcohol (50 mL) and the reaction mixture was allowed to stir at 0° C. for 12 h. The reaction mixture was quenched by the addition of sodium sulfite. The reaction mixture was diluted with water (500 mL) and ethyl acetate (500 mL). The aqueous phase was separated and extracted with ethyl acetate (2×200 mL). The combined organic extracts were washed with saturated aqueous sodium chloride (400 mL), dried (magnesium sulfate) and the solvent was removed in vacuo to give a crude oil. Purification by flash column chromatography (silica, ethyl acetate:hexanes 3:2) gave 16.75 g (92%, 32% ee) of (±)-3-[2-(benzyloxy)-3-tert-butylphenyl]propane-1,2-diol as a white solid. mp 79-81° C.; Anal. calcd. for C20H26O3: C, 76.4; H, 8.33. Found: C, 76.39; H, 8.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435837B2
Source datasetuspto-grants-2008_10
ORD IDord-bb00bd2dd2004bd5b2c01ba3024a51fd
Source noteuspto-grants-2008_10