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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705179Generated: October 29, 2026

Ethyl Acetate → HCID 71256589, compound

https://huagongshe.com/reaction/705179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant4-(Hydroxymethyl)benzeneboronic acidHCID 2734706—
Reactant2-Cyano-6-hydroxybenzothiazoleHCID 9881912—
SolventDimethylformamideHCID 6228—
ProductHCID 71256589HCID 7125658994.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Cyano-6-hydroxybenzothiazole (2) (150 mg, 0.85 mmol, 1.1 equiv.) and 4-(hydroxymethyl)benzeneboronic acid (5) (166 mg, 0.77 mmol, 1 equiv.) were dissolved in 15 mL dry dimethylformamide (DMF) prior to the addition of cesium carbonate (277 mg, 0.85 mmol, 1 equiv.). The mixture was stirred at 60° C. for 45-50 minutes before it was allowed to cool to room temperature. 100 mL EtOAc was added to the reaction mixture, and the organic phase was washed three times with DI H2O. The aqueous layers were combined and washed three times with EtOAc. All of the organic layers were combined, washed twice with brine, dried over sodium sulfate, and concentrated. The crude material was purified on a silica column (90:10 EtOAc:methanol, dry loaded) to give 225 mg (94%) of the pure product. 1H NMR (400 MHz, d6-Acetone): δ 5.33 (2H, s), 7.23 (2H, s), 7.45 (1H, dd, J=9.0, 2.6 Hz), 7.52 (2H, d, J=8.0 Hz), 7.93 (3H, m), 8.16 (1H, d, J=8.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173966B2
Source datasetuspto-grants-2015_11
ORD IDord-29218ff3441443239c503b53ab077ac0
Source noteuspto-grants-2015_11