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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853113Generated: October 29, 2026

N,N,N',N'-Tetramethylethylenediamine → 5,8-dimethylindeno[2,1-b]indol-6(5H)-one

https://huagongshe.com/reaction/853113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantCarbamic acid, N,N-dimethyl-, ethyl esterHCID 12709—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-methyl-3-(4-methylphenyl)-1H-indoleHCID 58931542—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product5,8-dimethylindeno[2,1-b]indol-6(5H)-oneHCID 11334116—

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of 2.19 g (0.00991 mol) of 1-methyl-3-(4-methylphenyl)-1H-indole and 3.24 mL (0.0218 mol) of TMEDA in 30 mL of ether was treated with 13.6 mL (0.0218 mol) of 1.6M BuLi in hexane under stirring at −40° C. Then the reaction mixture was allowed to warm up to r.t. and stirred for 4 h. The reaction mixture was cooled to −60° C. and treated with 1.16 g (0.00991 mol) ethyl N,N-dimethylcarbamate in 5 mL of ether. Then the reaction mixture was allowed to warm up to r.t. and was stirred overnight. Resulting mixture was treated with 50 mL of 10% aqueous NH4Cl. The violet precipitate was separated, washed twice with water and dried. Yield 1.04 g (42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253292B2
Source datasetuspto-grants-2007_08
ORD IDord-d0bea804a29e485190ab03ca9a96cc03
Source noteuspto-grants-2007_08