HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243854Generated: November 3, 2026
Ethyl 3-(N,N-dimethylamino)acrylate → HCID 69594764, compound
https://huagongshe.com/reaction/1243854
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-(N,N-dimethylamino)acrylate | HCID 121015 | — |
| Reactant | HCID 21928945 | HCID 21928945 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69594764 | HCID 69594764 | — |
Reaction Steps
0.27 g of 2-oxo-5,5-diphenylcyclohex-3-enylamine hydrochloride is dissolved in 3 cm3 of methanol and the solution is cooled to a temperature in the region of 0° C. 0.14 cm3 of ethyl 3-dimethylaminoacrylate is added to the preceding solution and the mixture is stirred for about 60 hours at a temperature in the region of 20° C. The reaction mixture is then concentrated to dryness under reduced pressure (13 kPa) and the residue is taken up in 12 cm3 of tetrahydrofuran. 0.3 g of ethyl 3-(2-oxo-5,5-diphenylcyclohex-3-enylamino)acrylate is obtained in the form of an orange-coloured oil, which is used without further modification in subsequent syntheses and the characteristics of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119115B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-d748d70cd9be41a8bcbdd529b2836b95 |
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| Source note | uspto-grants-2006_10 |
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