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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445936Generated: October 30, 2026

Trimethyl phosphonoacetate → HCID 59170459, compound

https://huagongshe.com/reaction/1445936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl phosphonoacetateHCID 80029—
ReactantHCID 59170456HCID 59170456—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59170459HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666898B2
Source datasetuspto-grants-2010_02
ORD IDord-39cf2dfd577b462a93c3011682fffed0
Source noteuspto-grants-2010_02