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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376110Generated: October 30, 2026

Ethyl Acetate → HCID 69007483, compound

https://huagongshe.com/reaction/1376110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1-Acetoxy-2-bromoethaneHCID 13564—
ReactantHCID 19360204HCID 19360204—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69007483HCID 6900748345%

Reaction Conditions

Temperature0 °C

Reaction Steps

Stir and cool to 0° C. a mixture of N-(5-chloro-2-cyanophenyl)acetamide (see Example 8, 1.0 g, 5.14 mmol) and THF (10 mL) and add potassium tert-butoxide (6.2 mL, of a 1M solution in THF) and stir at 0° C. for 30 min. Add bromoethyl acetate (0.6 mL) in one portion. Stir at room temperature for 2 h. Quench the reaction with water (40 mL) and stir with ethyl acetate. Separate the layers and reextract the aqueous with ethyl acetate. Combine the organic extracts and wash with water and brine. Dry over MgSO4 and concentrate under reduced pressure to obtain a brown solid. Triturate the solid with ether and collect a beige solid. Chromatograph the solid on silica gel with 2% ethyl acetate/dichloromethane followed by 10% ethyl acetate/dichloromethane to obtain 0.65 g (45%) of the title compound as a beige solid: MS 281(M+H), HPLC: Rt=3.20 min., TLC (silica gel, 10% ethyl acetate/dichloromethane) Rf=0.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169925B2
Source datasetuspto-grants-2007_01
ORD IDord-7c24a12b06f04439ab928568a7caaeea
Source noteuspto-grants-2007_01