Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842937Generated: October 30, 2026

Acetonitrile → HCID 68880526, compound

https://huagongshe.com/reaction/842937

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 numberUS06376533B1
Source datasetuspto-grants-2002_04
ORD IDord-42f35978db624c44849cde1f2f7100e4
Source noteuspto-grants-2002_04