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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904459Generated: October 31, 2026

Water → Methyl 4-[6-(2-ethylhexanamido)indol-1-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/1904459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-Ethylhexanoyl chlorideHCID 79103—
ReactantMethyl 4-(6-aminoindol-1-ylmethyl)-3-methoxybenzoateHCID 14708762—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-[6-(2-ethylhexanamido)indol-1-ylmethyl]-3-methoxybenzoateHCID 2003873799%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution of methyl ester (B) (0.5 g) in methylene chloride (16 ml) was cooled to 0° C. and treated with triethylamine (0.34 ml) followed by 2-ethylhexanoyl chloride (0.31 ml). The resulting solution was stirred at 0° C. for 15 minutes and then at room temperature for 30 minutes. The mixture was diluted with ethyl acetate and poured into cold water. The organic layer was washed sequentially with 10% v/v hydrochloric acid, water, and brine; dried (MgSO4) and evaporated. The residue was purified by flash chromatography on a 4×18 cm silica gel column using 35:65 v/v ethyl acetate:hexane as the eluent to give methyl 4-[6-(2-ethylhexanamido)indol-1-ylmethyl]-3-methoxybenzoate (C) (0.7 g; 99%) as a white solid; partial NMR: 0.9(t, 6H, 2CH3), 1.5(m, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837235
Source datasetuspto-grants-1989_06
ORD IDord-cb4cecfb6362403db8992f1b99b82c05
Source noteuspto-grants-1989_06