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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041883Generated: October 27, 2026

Methanol → Betulonal

https://huagongshe.com/reaction/2041883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantBetulinHCID 72326—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
ProductBetulonalHCID 4731116%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 250 ml round-bottomed flask, equipped with a magnetic stirring bar, a 100 ml addition funnel and a septum fitted with a nitrogen inlet, was placed 1 g (2.258 mmol) betulin in 150 ml acetone. The flask was cooled with an ice-acetone bath and the suspension of betulin was treated dropwise with Jones' reagent [L. F. Fieser, M. Fieser, Reagents for Organic Synthesis, vol. 1, 1967, p. 143] over 15 minutes. The reaction mixture was stirred at 0° C. for 2 hours and then treated with methanol (25 ml) until it turned dark green. The reaction mixture was poured onto a mixture of ice and water (50 ml), then acetone and methanol were removed under reduced pressure. The aqueous residue was extracted three times with 40 ml ethyl acetate. The combined organic extracts were washed first with water (20 ml) and then with brine (15 ml), then dried (MgSO4). The solvent was evaporated under reduced pressure to give a white solid. The crude residue was purified by chromatography on silica gel 60G (ethyl acetate/petroleum ether 40-60° C., 1/9 then 1/4) to yield first 59 mg (6%) betulonal as a white solid, then 880 mg (86%) betulonic acid 1 as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586569B2
Source datasetuspto-grants-2013_11
ORD IDord-b5635915052444b4a733f4a7aef54129
Source noteuspto-grants-2013_11