HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50051Generated: November 1, 2026
Triethylamine → HCID 17821889, compound
https://huagongshe.com/reaction/50051
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Chloromethyl)-2-propenenitrile | HCID 24308 | — |
| Reactant | Dimethyl (2-hydroxyethyl)phosphonate | HCID 2733833 | — |
| Catalyst | Phenothiazine | HCID 7108 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 17821889 | HCID 17821889 | 54.2% |
Reaction Steps
86.3 g (850 mmol) 2-(chloromethyl)-acrylonitrile are added dropwise at room temperature to a solution of 130.9 g (850 mmol) 2-hydroxyethylphosphonic acid dimethylester, 85.9 g (850 mmol) triethylamine (TEA) and 40 mg phenothiazine (stabilizer) in 1 l THF. Subsequently, the mixture is heated for 6 hours at 65° C. under reflux. 9.1 g (90 mmol) TEA and 9.1 g (90 mmol) 2-(chloromethyl)-acrylonitrile are once again added one after the other and the mixture is heated for a further 24 hours under reflux. After the reaction mixture has cooled, the formed deposit of TEA hydrochloride is filtered out and is washed twice with 50 ml THF. After the THF phases have been concentrated on the rotary evaporator, the residual raw product is taken up in 650 ml methylene chloride and washed twice with water. After it has been dried over anhydrous sodium sulphate, the mixture is concentrated and the residual liquid undergoes fractional distillation in the fine vacuum. 101.0 g (54% yield) of a colourless liquid results at b.p. 150° C. (0.05 mbar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06710149B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-28fc72b09bfd40d38c95cdc20e1e7b8f |
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| Source note | uspto-grants-2004_03 |
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