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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268461Generated: October 29, 2026

Methyl iodide → HCID 21552248, compound

https://huagongshe.com/reaction/268461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 21552259HCID 21552259—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 21552248HCID 21552248—

Reaction Steps

If the 3-(2'-methyl-2'-nitrobutyl)-5-methoxy-indole obtained as intermediate product in Example 2 is methylated by the procedure described in Example 4 (or by means of sodium hydride and methyl iodide in hexamethyl phosphoric acid triamide), 1-methyl-3-(2'-methyl-2'-nitrobutyl)-5-methoxy-indole is obtained and melts at 95°-96°C. after crystallisation from acetone/water and distillation. Catalytic reduction thereof yields 1-methyl-3-(2'-methyl-2'-aminobutyl)-5-methoxy-indole. Melting point of the benzoic acid salt 179.5°-184°C. (insoluble in ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947584
Source datasetuspto-grants-1976_03
ORD IDord-8fb34a85a61c4c2781aa6f678718e8bf
Source noteuspto-grants-1976_03