HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400990Generated: October 30, 2026
N,N,N',N'-Tetramethylethylenediamine → Diethyl 2,2-difluoropentanedioate
https://huagongshe.com/reaction/400990
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Diethyl 2,2-difluoropentanedioate | HCID 20455495 | 299.5% |
Reaction Steps
To a solution of ethyl bromodifluoroacetate (33.2 g) in tetrahydrofuran (94.0 g) was added ethyl acrylate (8.2 g) and copper powder (10.9 g). After heating to 50° C., TMEDA (9.5 g) was added dropwise and the reaction mixture was then stirred for 3 hours at the same temperature. Upon disappearance of ethyl acrylate as the starting material, to the reaction solution was added methyl t-butyl ether (MTBE, 73.7 g) followed by addition of 10% aqueous ammonium chloride solution (49.8 g) dropwise, and the mixture was then stirred for 30 minutes. The remaining copper residue was removed by filtration through a celite, and methyl t-butyl ether (MTBE, 66.3 g) was added to separate the layers. The separated organic layer was washed successively with 10% aqueous NH4Cl solution (66.3 g) and 3 N aqueous hydrochloric acid solution (99.6 g) in order and then distilled under reduced pressure to obtain 55.0 g of the desired title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741927B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-d94d99c1ee2a4b8f867711415bd0060a |
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| Source note | uspto-grants-2014_06 |
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