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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378368Generated: October 26, 2026

Methyl iodide → (1-Methyl-1H-indol-6-yl)methanol

https://huagongshe.com/reaction/378368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant6-HydroxymethylindoleHCID 2773459—
SolventDimethylformamideHCID 6228—
Product(1-Methyl-1H-indol-6-yl)methanolHCID 1867303275%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH(8.2 mm) in N,N-dimethylformamide ("DMF") (20 mL) was cooled to 0° C., then treated with a solution of the known 1H-indole-6-methanol (1 g,6.8 mm) in DMF(8 mL). After stirring for 1 hour at 0° C., methyl iodide ("MeI") (0.51 mL, 8.2 mm) dissolved in DMF (2 mL) was added, and the mixture was stirred at 0° C. overnight, then poured into ice/H2O(250 ml) and extracted with EtOAc(50 mL×3). The organic fraction was dried over MgSO4, filtered, evaporated and purified by flash column chromatography to afford 1-methyl-1H-indole-6-methanol (0.82 g. 75%). This product (1-methyl-1H-indole-6-methanol, 1 g, 6.2 mm) was dissolved in a mixture of pyridine (5 mL) and acetic anhydride (Ac2O) (5 mL) and stirred at room temperature overnight. The solvent was evaporated, and the residue purified by flash column chromatography to afford 1.09 g of Acetic acid 1-methyl-1H-indol-6-yl methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030994
Source datasetuspto-grants-2000_02
ORD IDord-707a1220dfcf4d82a55a6079f14296b7
Source noteuspto-grants-2000_02