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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583421Generated: October 28, 2026

Methyl iodide → HCID 53706700, compound

https://huagongshe.com/reaction/583421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 53876841HCID 53876841—
CatalystSilverHCID 23954—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 53706700HCID 53706700—

Reaction Steps

295 g of silver(l) oxide are added, with stirring, to a solution of 75 g of N-tert-butyloxycarbonyl-amino-3-(1-tert-butyloxycarbonyl-indol-3-yl)-propanecarboxylic acid methyl ester in 770 ml of N,N-dimethylformamide. 75 ml of methyl iodide are then added dropwise. The reaction mixture rises to a temperature of 40° and is stirred at room temperature for 2 days and then diluted with 800 ml of ethyl acetate, filtered and concentrated by evaporation. The residue is purified by chromatography (silica gel, hexane/ethyl acetate 3:2). In this way the title compound is obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929067
Source datasetuspto-grants-1999_07
ORD IDord-70e8f1dcdeae4339a510a5b7e51d7150
Source noteuspto-grants-1999_07