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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Carbamic acid, N,N-dimethyl-, ethyl ester | HCID 12709 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Methyl-4-phenylthiophene | HCID 11401061 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-methyl-8H-indeno[2,1-b]thiophen-8-one | HCID 11275671 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253292B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-158b5e56f52949218843fdf63d27806a |
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| Source note | uspto-grants-2007_08 |
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