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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853112Generated: October 31, 2026

N,N,N',N'-Tetramethylethylenediamine → 2-methyl-8H-indeno[2,1-b]thiophen-8-one

https://huagongshe.com/reaction/853112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantCarbamic acid, N,N-dimethyl-, ethyl esterHCID 12709—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Methyl-4-phenylthiopheneHCID 11401061—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product2-methyl-8H-indeno[2,1-b]thiophen-8-oneHCID 11275671—

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of 12.88 g (0.074 mol) of 2-methyl-4-phenylthiophene, 23.4 mL (0.16 mol) of TMEDA in 200 mL of diethyl ether (ether) was treated with 100 mL (0.16 mol) of 1.6M BuLi in hexane under stirring at −40° C. Then the reaction mixture was allowed to warm up to room temperature (r.t.) and was stirred for 3 h (white precipitate forms). The reaction mixture was cooled to −40° C. and treated with 8.76 g (0.075 mol) of ethyl N,N-dimethylcarbamate in 25 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, the organic layer was separated and the organic phase was washed with 10% aqueous solution of NH4Cl and then dried by anhydrous Na2SO4. Solvent was evaporated and the residue was washed with methanol. Yield 6.8 g (46%) of red crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253292B2
Source datasetuspto-grants-2007_08
ORD IDord-158b5e56f52949218843fdf63d27806a
Source noteuspto-grants-2007_08