Trimethyl phosphonoacetate → HCID 59170459, compound

(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

1. additionAfter addition the mixture
2. stirringThe reaction mixture was stirred for 2 h at room temperature
3. concentrationThe mixture was concentrated
4. dissolutionredissolved in ethyl acetate (200 L)
5. washThe mixture was washed with 1 M HCl solution
6. dry with materialThe organic solution were dried over MgSO4
7. filtrationfiltered
8. concentrationconcentrated

ORD record

ord-39cf2dfd577b462a93c3011682fffed0

Source dataset

uspto-grants-2010_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07666898B2