HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404339Generated: November 1, 2026
tert-Butyl acrylate → HCID 66678183, compound
https://huagongshe.com/reaction/2404339
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Benzonitrile, 3-(((1-methylethyl)amino)methyl)- | HCID 485406 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66678183 | HCID 66678183 | — |
Reaction Steps
A mixture of 3-[(isopropylamino)methyl]benzonitrile (5.7 g, 32.7 mmol), tert-butyl acrylate (4.78 ml, 32.7 mmol) and DBU (5.0 ml, 32.7 mmol) was heated neat at 80° C. for 24 hours. The reaction mixture was diluted with water and extracted with DCM. The organic layer was dried over sodium sulfate and concentrated under reduced pressure. After purification by chromatography (silica, pet ether/EtOAc), the title compound was obtained as a colorless oil. 1H NMR (DMSO-d6, 400 MHz) δ 7.73 (s, 1H,), 7.67 (d, J=7.7 Hz, 1H), 7.63 (d, J=7.8 Hz, 1H), 7.49 (t, J=7.7 Hz, 1H), 3.56 (s, 2H), 2.75 (m, 1H), 2.62 (t, J=6.5 Hz, 2H), 2.25 (t, J=6.4 Hz, 2H), 1.39 (s, 9H), 0.83 (d, J=8.8 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802704B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-463a952000b04fb0aca6cafe53ce7431 |
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| Source note | uspto-grants-2014_08 |
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