Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006303Generated: November 1, 2026

Ethyl Acetate → HCID 11413280, compound

https://huagongshe.com/reaction/1006303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium SulfiteHCID 24437—
Reactant9-Decenyl acetateHCID 39801—
ReactantPotassium hydroxy sulfiteHCID 23707502—
CatalystOsmium TetroxideHCID 30318—
SolventDimethylformamideHCID 6228—
ProductHCID 11413280HCID 1141328093%

Reaction Steps

9-Decenyl acetate (100 mg) was dissolved in DMF (10 mL), and OsO4 (0.06 mL, 2.5% in tBuOH) was added and stirred for 5 min. OXONE (1.23 g) was added in one portion and the reaction had a final volume (12 mL). The reaction was stirred at room temperature for 3 hours or until the solution becomes colorless. This usually marks the completion of the reaction which was verified by TLC or GC. Na2SO3 (600 mg) was added, to reduce the remaining Os(VIII), and stirred for an additional hour or until solution became dark brown/black. EtOAc was added to extract the products and 1N HCl was used to dissolve the salts. The organic extract was washed with 1N HCl (50 mL×3) and brine (50 mL), dried over Na2SO4, and the solvent was removed under reduced pressure to obtain the crude product. 9-Acetoxy nonanoic acid was obtained in 93% yield without the need for further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787671B2
Source datasetuspto-grants-2004_09
ORD IDord-c7b5223da4b74eea82eff0e335525a82
Source noteuspto-grants-2004_09