Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484256Generated: October 25, 2026

1-Iodohexane → 5-(Hexyloxy)-2-methyl-1H-indole-3-acetic acid

https://huagongshe.com/reaction/484256

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodohexaneHCID 12527—
ReactantSodium MethoxideHCID 10942334—
ReactantO-Desmethyl-N-deschlorobenzoyl IndomethacinHCID 11310252—
SolventMethanolHCID 887—
Product5-(Hexyloxy)-2-methyl-1H-indole-3-acetic acidHCID 1993575762%

Reaction Steps

To a solution of 5-hydroxy-2-methyl-1H-indole-3-acetic acid (7.17 g, 35.0 mmol) in methanol (40 mL) is added sodium methoxide (70 mmol). The solution is evaporated, dimethylformamide (40 mL) is added followed by hexyl iodide (35.0 mmol). After 2 days the solvent is removed and the residue is partitioned between ethyl acetate and pH=4 buffer. The organic layer is separated, dried over MgSO4 and evaporated to 8.6 g of a brown solid. Recrystallization from ethanol/water affords 6.23 g (62%) of white crystals, m.p. 65°-67° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05229516
Source datasetuspto-grants-1993_07
ORD IDord-1e2dbac9c99d4930a37317edb68511d2
Source noteuspto-grants-1993_07