HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341334Generated: October 27, 2026
Ethyl cyanoacetate → HCID 71530805, compound
https://huagongshe.com/reaction/341334
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (Iodomethyl)trimethylsilane | HCID 77877 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 71530805 | HCID 71530805 | 83.5% |
Reaction Steps
A solution of ethyl cyanoacetate (5.34 g, 47.3 mmol) in dimethyl sulfoxide (DMSO, 20 ml) was added portionwise with sodium ethoxide (3.21 g, 47.2 mmol), and the mixture was stirred at room temperature for 4 hours with occasionally cooling the mixture on ice when temperature elevation was observed. The reaction mixture was put on an ice bath, and added dropwise with a solution of iodomethyltrimethylsilane (7.78 g, 36.4 mmol) in DMSO (5 ml), and the mixture was stirred at room temperature for 24 hours. The reaction mixture was added with saturated aqueous ammonium chloride, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate, and the solvent was evaporated. The residue was purified by silica gel chromatography [hexane/ethyl acetate (49:1)] to obtain ethyl 3-(trimethylsilyl)-2-cyanopropionate (6.06 g, 65%) mentioned in the title as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895769B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-98ad2bde8c044412b36dde6be0e975e6 |
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| Source note | uspto-grants-2014_11 |
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