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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293606Generated: November 1, 2026

Sodium hydride → HCID 21476978, compound

https://huagongshe.com/reaction/2293606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-IodopropaneHCID 33643—
ReactantHCID 21476971HCID 21476971—
ReactantHCID 21476972HCID 21476972—
SolventDimethylformamideHCID 6228—
ProductHCID 21476978HCID 2147697847%

Reaction Steps

Ethyl 1-(2-Carboethoxymethoxy-4-methoxybenzyl)-3-(3,4-methlenedioxyphenyl)-5-(prop-1-yloxy)indole-2-carboxylate. To a solution of ethyl 1-(2-carboethoxymethoxy-4-methoxybenzyl)-5-hydroxy-3-(3,4-methylenedioxyphenyl)indole-2-carboxylate (175 mg, 0.30 mmol) in DMF stirred at ice bath temperature under an argon atmosphere was added a slurry of NaH (11 mg of 80% oil dispersion, 0.36 mmol, oil removed by pentane wash) in DMF (1 mL). After 15 min at ice bath temperature, 1-iodopropane (0.255 g, 1.5 mmol) was added and the ice bath was removed. The reaction mixture was stirred an additional 30 min at room temperature then partitioned between 3N HCl (25 mL) and EtOAc (75 mL). The organic extract was washed successively with H2O, aqueous NaHCO3, H2O and saturated aqueous NaCl and dried (Na2SO4). The solvent was removed in vacuo and the resulting solid crystallized from EtOH to afford the title compound (83 mg 47%); m.p. 89°-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686481
Source datasetuspto-grants-1997_11
ORD IDord-2d3b872481914e04ba2687623c54f4d0
Source noteuspto-grants-1997_11