HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526432Generated: October 28, 2026
Hydrochloric Acid → Ethyl 2-(4-cyano-2-methoxyphenyl)-3-(dimethylamino)acrylate
https://huagongshe.com/reaction/526432
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Dimethylformamide diethylacetal | HCID 70913 | — |
| Reactant | Ethyl 2-(4-cyano-2-methoxyphenyl)acetate | HCID 117600541 | — |
| Reactant | Tert-butyl 2-(4-cyano-2 methoxyphenyl)acetate | HCID 117601441 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-(4-cyano-2-methoxyphenyl)-3-(dimethylamino)acrylate | HCID 117601030 | 74% |
Reaction Steps
Combined tert-butyl 2-(4-cyano-2-methoxyphenyl)acetate (549 mg, 2.218 mmol) and 4N HCl in dioxane (0.277 mL, 1.109 mmol) in ethanol (7.4 mL) and stirred for 16 hours at 60° C. The reaction was concentrated by rotary evaporation and then combined with ethyl 2-(4-cyano-2-methoxyphenyl)acetate (0.486 g, 2.217 mmol) and 1,1-diethoxy-N,N-dimethylmethanamine (1.9 mL, 11.08 mmol) in DMF (4.43 mL) and stirred for 16 hours at 100° C. The reaction mixture was diluted with 200 mL EtOAc and washed twice with 200 mL water. Organic layer was dried with sodium sulfate and concentrated to give a residue which was purified on a 60 g NH silica gel column eluting with hexanes and EtOAc to give the title compound (405 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345713B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8e16190dd5b04168948c0b4c0bd1e4ca |
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| Source note | uspto-grants-2016_05 |
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