HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174439Generated: October 30, 2026
Tetrahydrofuran → p-Benzyl-ethylaminophenethyl acrylate
https://huagongshe.com/reaction/1174439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chloride acrylate | HCID 21924244 | — |
| Reactant | p-Benzyl-ethylaminophenethyl alcohol | HCID 68771578 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | p-Benzyl-ethylaminophenethyl acrylate | HCID 68771319 | — |
Reaction Steps
In a three-aperture flask, 6.64 g (26 mmol) of p-benzyl-ethylaminophenethyl alcohol, 5.79 g (57.2 mmol) of triethylamine, and 50 mL of dehydrated tetrahydrofuran were poured, and the mixture was stirred under an argon atmosphere and an ice-cooling condition. Then, 4.70 g (52 mmol) of chloride acrylate was delivered by drops into the reaction solution for 30 minutes. Upon completion of the dripping, the reaction solution was further stirred for 3 hours. The reaction solution was poured to 100 mL of water and then an extract was obtained therefrom by using toluene, followed by washing with water three times. The toluene solution was dried with anhydrous magnesium sulfate, and then the solvent was distilled away to purify the toluene solution by silica gel chromatography using a mixture solvent of hexane/ethyl acetate (5/1) as an eluent to thereby synthesize 3.21 g (yield: 40% by mass) of p-benzyl-ethylaminophenethyl acrylate of the exemplified compound No. 22 represented by the following structural formula.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838188B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-1c94f8146a6741abbe04370430a8594a |
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| Source note | uspto-grants-2010_11 |
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