HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → 1-[4-(Carboxymethoxy)benzyl]-3-dodecanoylindole-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 2-Methylpropan-2-olate | HCID 4574913 | — |
| Reactant | 1H-Indole-2-carboxylic acid, 3-(1-oxododecyl)-, ethyl ester | HCID 10619240 | — |
| Reactant | Ethyl 2-[4-(bromomethyl)phenoxy]acetate | HCID 12870369 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[4-(Carboxymethoxy)benzyl]-3-dodecanoylindole-2-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06310217B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-051fa19db58d463f85a8a8f8c2582f58 |
| Source note | uspto-grants-2001_10 |