HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821005Generated: October 31, 2026
tert-Butyl acrylate → HCID 68893121, compound
https://huagongshe.com/reaction/1821005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Reactant | Bis(cyclohexylmethyl)amine | HCID 4594378 | — |
| Reactant | HCID 69017910 | HCID 69017910 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68893121 | HCID 68893121 | — |
Reaction Steps
In an oven-dried flask, under an atmosphere of argon, 10 mg of 2-(di-tert-butylphosphino)biphenyl (0.03 mmol) and 13 mg of tris(dibenzylideneacetone)-dipalladium-chloroform complex (0.015 mmol) were dissolved in 10 mL of anhydrous dioxane and the solution was degassed with argon. To this mixture, 100 μL of N,N-dicyclohexylmethylamine (0.45 mmol), 55 μL of tert-butyl acrylate (0.38 mmol), and a dioxane (1 mL) solution of 125 mg (0.30 mmol) of 2-(3-cyano-4-isopropyloxyphenyl)-5-(4-bromo-2-methyphenyl)-1,3,4-thiadiazole (from Step B) were added sequentially via syringe. The resulting mixture was heated under argon atmosphere at 95° C. for 2 h. The reaction mixture was diluted with 20 mL of EtOAc, filtered trough a disposable frit and concentrated. Pure product was isolated by a column chromatography, using Biotage 40S column (eluent: hexanes/EtOAc=4/1) as a mixture of (E)- and (Z)-stereoisomers: 1H NMR (500 MHZ, CDCl3, major, (E)-stereoisomer) δ 1.46 (d, J=6.5, 6H), 2.69 (s, 3H), 4.79 (sep, J=6.5, 1H), 6.47 (d, J=15.5, 1H), 7.12 (d, J=9.0, 1H), 7.51 (d, J=9.0, 1H), 7.52 (s, 1H), 7.61 (d, J=15.5, 1H), 7.80 (d, J=8.0, 1H), 8.18 (d, J=2.0, 1H), 8.25 (dd, J=8.0, 2.0, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605171B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-3a048523913142558faa3b4f0ec15190 |
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| Source note | uspto-grants-2009_10 |
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