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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220326Generated: November 1, 2026

Dimethyl Sulfate → 7-Benzyloxy-1-methylindole

https://huagongshe.com/reaction/2220326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium SulfateHCID 24436—
Reactant7-(Benzyloxy)-1H-indoleHCID 260798—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product7-Benzyloxy-1-methylindoleHCID 22136813—

Reaction Steps

To a solution of 7-benzyloxy-1H-indole (Ref: Dobson, D; Todd, A; Gilmore, J. Synth. Commun. (1991), 21(5), 611-17) (1.29 g, 5.78 mmol) in ethanol (30 mL) was added potassium hydroxide (0.41 g, 7.23 mmol) and dichloromethane (5 mL) of to help solubilize the starting material. The resulting solution was allowed to stir at room temperature for 10 min before evaporating the solvent in vacuo. The residue was taken up in acetone (75 mL) and sodium sulfate (4.9 g, 34.7 mmol) was added followed by dimethyl sulfate via syringe (0.62 mL, 6.3 mmol). The solution was stirred for 1 h, then filtered and evaporated in vacuo. This material was purified by flash chromatography, eluting silica gel with hexane: ethyl acetate (100:0 to 10:1) to give the product. (1.12 g, 82%); Mass spectrum (ion spray): m/z=238.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417064B2
Source datasetuspto-grants-2008_08
ORD IDord-754948cccc52410e9039e5d04c093d40
Source noteuspto-grants-2008_08