HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480532Generated: October 30, 2026
Pyridine → 2-(Trimethylsilyl)ethyl 2-methylprop-2-enoate
https://huagongshe.com/reaction/480532
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | 2-(Trimethylsilyl)ethanol | HCID 18013 | — |
| Catalyst | Phenothiazine | HCID 7108 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Trimethylsilyl)ethyl 2-methylprop-2-enoate | HCID 22335777 | 44.7% |
Reaction Steps
2-Trimethylsilylethanol (Aldrich) (30 g, 0.25 mole) was placed in a round bottom flask equipped with a condenser, addition funnel, magnetic stirrer and a nitrogen inlet. 200 ml dichloromethane, pyridine (20.80 g, 0.26 mole) and 100 mg of phenothiazine were added to the flask. While stirring, methacryloyl chloride (27.18 g, 0.26 mole) in 100 ml dichloromethane was added dropwise at room temperature. A mildly exothermic reaction occurred. The mixture was stirred overnight at room temperature. Afterwards, the mixture was washed with 1×100 ml deionized water and 2×100 ml brine and dried over anhydrous magnesium sulfate. The solution was concentrated in vacuo. Fractional distillation under reduced pressure gave 20.82 grams of the desired product at 35-38° C. at 0.5 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06653048B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-5c41783623f34f609e6c00c17305d884 |
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| Source note | uspto-grants-2003_11 |
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