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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50009Generated: October 28, 2026

Acetonitrile → HCID 68880526, compound

https://huagongshe.com/reaction/50009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantCyclobutanecarboxylic acid, 1-(hydroxy-2-thienylmethyl)-, ethyl esterHCID 12080529—
ProductHCID 68880526HCID 68880526—

Reaction Conditions

Temperature23 °C

Reaction Steps

Trimethylsilyliodide (20 g, 100 mmol) was added to CH3CN (10 mL) at 0° C. and the mixture was allowed to stir 5 min. A solution of alcohol 2 (5 g, 20 mmol) in CH3CN (10 mL) was added slowly while the temperature was kept between 4-10° C. and the reaction was allowed to warm to 23° C. After stirring for 2 h at 23° C. the reaction was judged complete via TLC analysis. The mixture was poured into 3N NaOH at 0° C. and EtOAc was added. The organic layer was separated, washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. FCC (silica gel, 1:1 hexane/CH2Cl2) gave 2.3 g of the above named ester 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710072B2
Source datasetuspto-grants-2004_03
ORD IDord-0217d9ac8db847a3b85531c5faa9f88b
Source noteuspto-grants-2004_03