HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194740Generated: October 31, 2026
Sodium hydride → 2-(2,2,2-Trifluoro-ethyl)-malonic acid dibenzyl ester
https://huagongshe.com/reaction/2194740
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,2,2-Trifluoroethyl trifluoromethanesulfonate | HCID 80366 | — |
| Reactant | Dibenzyl malonate | HCID 84754 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2,2,2-Trifluoro-ethyl)-malonic acid dibenzyl ester | HCID 67050488 | 68% |
Reaction Steps
To a suspension of 60% sodium hydride (0.678 g, 16.97 mmol) in THF (100 mL) at room temperature was added malonic acid dibenzyl ester (4.825 g, 16.97 mmol) to give a clear solution after 30 min. Trifluoro-methanesulfonic acid 2,2,2-trifluoro-ethyl ester (3.52 g, 15.43 mmol) was added and reaction mixture was stirred at 50° C. for 48 h. The reaction mixture was concentrated, partioned between ethyl ether and washed with saturated ammonium chloride solution and acidified with 1N HCl. The mixture was extracted with ethyl ether (2×), dried (MgSO4), and concentrated. The resulting residue was purified by flash column chromatography (silica gel, 0 to 0% ethyl ether/hexanes) to give a colorless oil (3.844 g, 68%). 1H NMR (300 MHz, CDCl3): δ 7.4-7.2 (m, 10H), 5.15 (s, 4H), 3.75 (t, J=6.9 Hz, 1H), 2.9-7.7 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08334295B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-292d7016cbf04211ab1d980b67dc5fe0 |
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| Source note | uspto-grants-2012_12 |
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