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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258450Generated: October 30, 2026

Acetic Acid → (3R,4S,7S) 3,7-dibenzyloxy-4-vinyldodeca-5-enecarboaldehyde

https://huagongshe.com/reaction/258450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
Reactant(3 R,4S,7S) 3,7-dibenzyloxy-4-vinyl-1,1-dimethoxydodeca-5-eneHCID 67862608—
SolventTetrahydrofuranHCID 8028—
Product(3R,4S,7S) 3,7-dibenzyloxy-4-vinyldodeca-5-enecarboaldehydeHCID 86746684—

Reaction Steps

While stirring, 776 mg (1.67 mM) of (3R,4S, 7S) 3,7-dibenzyloxy-4-vinyl-1,1-dimethoxydodeca-5-ene [8] described above was heated in a mixture of 13 ml of 80% acetic acid and 2 ml of tetrahydrofuran at 40° C. for 5 hours. Completion of the reaction was confimred by thin layer chromatography. Then, the reaction solution was poured into saturated sodium bicarbonate aqueous solution. The mixture was extracted 3 times with a solvent mixture of diethyl ether:hexane=7:3. The extracts were combined and washed sequentially with saturated sodium bicarbonate aqueous solution and saturated sodium chloride aqueous solution. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure to give 701 mg (1.67 mM) of (3R,4S,7S) 3,7-dibenzyloxy-4-vinyl-dodeca-5-enecarboaldehyde [9]. Yield, 100%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05266703
Source datasetuspto-grants-1993_11
ORD IDord-db4730de99994e1fba2398c90c12c162
Source noteuspto-grants-1993_11