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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Carbamic acid, N,N-dimethyl-, ethyl ester | HCID 12709 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-[4-(Tert-butyl)phenyl]-2-methylthiophene | HCID 11447572 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 6-(tert-butyl)-2-methyl-8H-indeno[2,1-b]thiophen-8-one | HCID 11817717 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07253292B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-505610f2e8ee4cdf84050ced6cd31fc9 |
|---|
| Source note | uspto-grants-2007_08 |
|---|