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
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 | 1-methyl-3-(4-methylphenyl)-1H-indole | HCID 58931542 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5,8-dimethylindeno[2,1-b]indol-6(5H)-one | HCID 11334116 | — |
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
| 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-d0bea804a29e485190ab03ca9a96cc03 |
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| Source note | uspto-grants-2007_08 |
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