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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342737Generated: October 27, 2026

Sodium ethoxide → 1-[4'-(4"-Chlorophenyl)phenyl]-3,3-dicarboethoxy-1-oxo-7-phenylheptane

https://huagongshe.com/reaction/342737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
Reactant(4-Iodobutyl)benzeneHCID 12709818—
ReactantEthyl 2-carboethoxy-4[4'-(4"-chlorophenyl)phenyl]-4-oxobutanoateHCID 22116404—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1-[4'-(4"-Chlorophenyl)phenyl]-3,3-dicarboethoxy-1-oxo-7-phenylheptaneHCID 5437143156.1%

Reaction Steps

Ethyl 2-carboethoxy-4[4'-(4"-chlorophenyl) phenyl]-4-oxobutanoate (0.40 g, 1.02 mmol) was added in one portion at rt to a solution of sodium ethoxide (0.08 g, 1.12 mmol) in DME (1 mL). After 15 min, 4-phenyl-1-iodobutane (0.24 g, 0.93 mmol) in DME (3 mL) was added. The resulting solution was stirred for 18 h. The solvent was concentrated in vacuo and the resulting oil dissolved in CH2Cl2 (100 mL) and washed with water (100 mL). The phases were separated and the aqueous phase was extracted with CH2Cl2 (2×50 mL). The combined organic phases were dried (MgSO4), filtered, and concentrated in vacuo. The resulting oil was purified by flash chromatography on silica gel using a gradient of ethyl acetate/hexane (10% to 25% ethyl acetate) as the eluent to afford a crystalline solid which was recrystallized with hexane and ethyl acetate to afford 1-[4'-(4"-chlorophenyl)phenyl]-3,3-dicarboethoxy-1-oxo-7-phenylheptane (0.272 g, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859047
Source datasetuspto-grants-1999_01
ORD IDord-56bc0e55120b446cb67dd607bc3b4009
Source noteuspto-grants-1999_01