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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006279Generated: November 2, 2026

Ethyl acetate hexane → HCID 22676834, compound

https://huagongshe.com/reaction/1006279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 22676749HCID 22676749—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22676834HCID 2267683499%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a dry 100 mL and stir bar was charged with 4.70 g ethyl 6-(benzoyloxy)-1-(phenylsulfonyl)indole carboxylate (Example 210) and dissolved in 12.5 mL of anhydrous tetrahydrofuran then cooled to 0° C. To this rapidly stirring solution was added 35.0 mL 1.0 M tetrahydrofuran solution of potassium tert-butoxide dropwise via syringe. Upon complete addition the contents were warmed to room temperature and stirred an additional ½ hour then quenched with 10 mL of 3N HCl solution followed by addition of 30 mL of water. The reaction was extracted with 3×50 mL of ethyl acetate then dried over Na2SO4 and concentrated in vacuo. The crude material was purified via column chromatography to yield 3.28g (99.0% yield) of an off white solid. The product had a Rf of 0.42 20% ethyl acetate/hexane; 1H NMR (300 MHz, Acetone-D6); 8.80 Hz, (s, 1H), 8.02 Hz, (dd, 1H), 7.95 Hz, (dd, 1H), 7.68 Hz, (dd, 1H), 7.58 Hz, (m, 2H), 7.46 Hz, (d, 2H), 7.21 Hz, (d, 1H), 6.87 Hz, (dd, 1H), 4.31 Hz (q, 2H), 1.31 Hz (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787651B2
Source datasetuspto-grants-2004_09
ORD IDord-363f4294283f4df1b1585d74640e99b0
Source noteuspto-grants-2004_09