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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853116Generated: October 30, 2026

N,N,N',N'-Tetramethylethylenediamine → 6-(tert-butyl)-2-methyl-8H-indeno[2,1-b]thiophen-8-one

https://huagongshe.com/reaction/853116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantCarbamic acid, N,N-dimethyl-, ethyl esterHCID 12709—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-[4-(Tert-butyl)phenyl]-2-methylthiopheneHCID 11447572—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product6-(tert-butyl)-2-methyl-8H-indeno[2,1-b]thiophen-8-oneHCID 11817717—

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of 2.23 g (0.01 mol) of 4-[4-(tert-butyl)phenyl]-2-methylthiophene, 2.97 mL (0.02 mol) of TMEDA in 30 mL of ether was treated with 13 mL (0.02 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 3 h. The reaction mixture was cooled −40° C. and treated with 1.17 g (0.01 mol) of ethyl N,N-dimethylcarbamate in 10 mL of ether. Then the reaction mixture was allowed to warm up to r.t. and was stirred overnight. Resulting mixture was treated with 10% aqueous NH4Cl, organic layer was separated, washed with 10% aqueous NH4Cl and then dried over anhydrous Na2SO4. Solvent was evaporated, the residue was washed with methanol. Yield 2.4 g (about 100%) of red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253292B2
Source datasetuspto-grants-2007_08
ORD IDord-505610f2e8ee4cdf84050ced6cd31fc9
Source noteuspto-grants-2007_08