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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856006Generated: October 31, 2026

Dimethylamine → HCID 23347374, compound

https://huagongshe.com/reaction/1856006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantFormaldehydeHCID 712—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Isopropyl-1H-indoleHCID 87307—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 23347374HCID 23347374—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a well-stirred solution of 2-isopropylindole (9.9 g.) in ethanol (30 ml.) at 0° C., there was added a 33% (w./w.) solution of dimethylamine in ethanol (10 ml.) and glacial acetic acid (3.5 ml.). A solution of 40% (w./v.) aqueous formaldehyde (5 ml.) was then added dropwise to the mixture, and the resulting solution was stirred at 5° C. for a period of one hour. Ice/water was next added to the reaction mixture, followed by excess solid potassium carbonate to give an orange oil. The liquid was then repeatedly extracted with diethyl ether (three times), using 50 ml. portions for each extraction. The combined ethereal extracts were then dried over anhydrous sodium sulfate and evaporated to give crude 3-(dimethylaminomethyl)-2-isopropylindole (4.5 g.) as a brown oil. The latter substance was used directly in Example I (as a starting material) without any further purification being necessary.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04217357
Source datasetuspto-grants-1980_08
ORD IDord-e34c01c06c2a42a3a33daa63fcdbf48a
Source noteuspto-grants-1980_08