Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382828Generated: October 30, 2026

Sodium Chloride → 1-[4-(Carboxymethoxy)benzyl]-3-dodecanoylindole-2-carboxylic acid

https://huagongshe.com/reaction/382828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant2-Methylpropan-2-olateHCID 4574913—
Reactant1H-Indole-2-carboxylic acid, 3-(1-oxododecyl)-, ethyl esterHCID 10619240—
ReactantEthyl 2-[4-(bromomethyl)phenoxy]acetateHCID 12870369—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product1-[4-(Carboxymethoxy)benzyl]-3-dodecanoylindole-2-carboxylic acidHCID 18362064—

Reaction Steps

A mixture of 223 mg (0.6 mmol) of ethyl 3-dodecanoylindole-2-carboxylate, 81 mg (0.72 mmol) of potasisum t-butoxide and 2 ml of absol. DMSO is stirred in an oil bath at 110° C. for 5 min. Then 197 mg (0.72 mmol) of ethyl 2-[4-(bromomethyl)phenoxy]acetate are added, and the mixture is heated at the same temperature for a further 10 min. Cooling and addition of water and NaCl are followed by extraction with ether. The organic phase is dried over Na2SO4, the solvent is distilled off, and the residue is chromato-graphed on silica gel with petroleum ether/ethyl acetate (9+1). The resulting ethyl 3-dodecanoyl-1-{4-[(ethoxycarbonyl)methoxy]benzyl}indole-2-carboxylate is hydrolyzed in analogy to Example 2E. The product is precipitated from ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310217B1
Source datasetuspto-grants-2001_10
ORD IDord-051fa19db58d463f85a8a8f8c2582f58
Source noteuspto-grants-2001_10