HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415483Generated: November 1, 2026
Water → (Z)-3-(4-bromo-3-methoxy-phenylamino)-but-2-enoic acid ethyl ester
https://huagongshe.com/reaction/2415483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | 4-Bromo-3-methoxyaniline | HCID 7018254 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | (Z)-3-(4-bromo-3-methoxy-phenylamino)-but-2-enoic acid ethyl ester | HCID 69287166 | 68.9% |
Reaction Steps
7.66 g (37.9 mmol) of 4-bromo-3-methoxy-phenylamine (preparation described in Tetrahedron Lett., 1995, 7583) were dissolved in 80 ml of cyclohexane at 70° C. and subsequently treated under stirring with 72 mg (0.38 mmol) of p-toluenesulfonic acid monohydrate and 4.93 g (37.9 mmol) of ethyl acetoacetate. The solution was then heated at reflux for 3.5 h with a water separator funnel connected. It was then cooled to RT and concentrated in vacuo. The residue was applied to a silica gel column with hexane/diethyl ether (3:1) as eluent. Combinations of the purified fractions and concentration in vacuo gave 8.2 g (68.8%) of the (Z)-3-(4-bromo-3-methoxy-phenylamino)-but-2-enoic acid ethyl ester, as a yellow solid. ISP mass spectrum, m/e: 316.2(M+1 calculated for C13H16BrNO3: 316).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06818767B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-e6c9897c8f6d498fb4fa75927f0a7fee |
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| Source note | uspto-grants-2004_11 |
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