HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445936Generated: October 30, 2026
Trimethyl phosphonoacetate → HCID 59170459, compound
https://huagongshe.com/reaction/1445936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl phosphonoacetate | HCID 80029 | — |
| Reactant | HCID 59170456 | HCID 59170456 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59170459 | HCID 59170459 | — |
Reaction Steps
(E)-methyl 3-(1-benzyl-5-ethyl-1H-pyrrol-2-yl)acrylate, 15: Sodium (0.75 g, 32 mmol) was added in portions to a dry methanol (30 mL). To the fresh formed sodium methoxide solution was added dropwise the solution of trimethyl phosphonoacetate (2.6 mL, 15.2 mmol) in tetrahydrofuran (7 mL) at room temperature. After addition the mixture was stirred for additional 60 min at room temperature. Then to the reaction mixture was added dropwise the solution of 1-benzyl-5-ethyl-1H-pyrrole-2-carbaldehyde, 14 (2 g) in tetrahydrofuran (50 mL) at room temperature. The reaction mixture was stirred for 2 h at room temperature. The mixture was concentrated and redissolved in ethyl acetate (200 L). The mixture was washed with 1 M HCl solution, then saturated NaHCO3, H2O. The organic solution were dried over MgSO4 and then filtered, concentrated to afford the crude product, (E)-methyl 3-(1-benzyl-5-ethyl-1H-pyrrol-2-yl)acrylate, 15.Yield: 2 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666898B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-39cf2dfd577b462a93c3011682fffed0 |
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| Source note | uspto-grants-2010_02 |
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