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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37707Generated: October 26, 2026

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

https://huagongshe.com/reaction/37707

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 numberUS05420289
Source datasetuspto-grants-1995_05
ORD IDord-2918c717de254b449985b0c368a94450
Source noteuspto-grants-1995_05