HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370474Generated: October 30, 2026
Dimethyl Sulfate → Methyl 2-methoxy-3-(3-nitrophenyl)prop-2-enoate
https://huagongshe.com/reaction/2370474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 66905811 | HCID 66905811 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-methoxy-3-(3-nitrophenyl)prop-2-enoate | HCID 66905787 | 68.3% |
Reaction Steps
Dimethyl sulfate (13.23 g, 105 mmol) was added to a stirred mixture of 2-hydroxy-3-(3-nitrophenyl)acrylic acid (10.5 g, 50.0 mmol) and caesium carbonate (39.1 g, 120 mmol) in DMF (105 ml) to form a clear, pale yellow mixture, which was stirred at RT overnight. The resulting dark red suspension was concentrated in vacuo and the residue partitioned between water (100 ml) and dichloromethane (150 ml). The organic layer was separated, further washed with water (2×100 ml), dried over sodium sulphate and filtered through silica gel. The resulting yellow solution was evaporated to dryness in vacuo to give methyl 2-methoxy-3-(3-nitrophenyl)acrylate as a yellow solid (8.1 g, 67%). 1H NMR (δ, 250 MHz, DMSO-d6)=3.81 (3H, s), 3.83 (3H, s), 7.08 (1H, s), 7.71 (1H, dd, 7.9 & 8.2 Hz), 8.10-8.22 (2H, m), 8.66 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710100B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-3073baac63bd45ed950f7707ca3e848b |
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| Source note | uspto-grants-2014_04 |
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