HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 10592900, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(1H-Pyrrol-1-Yl)Phenol | HCID 712334 | — |
| Reactant | HCID 13608722 | HCID 13608722 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10592900 | HCID 10592900 | 54.9% |
Reaction Steps
Sodium hydride (90 mg, 3.9 mmol) was added to a solution of 1-(2-hydroxyphenyl)pyrrole (0.41 g, 2.5 mmol) in anhydrous THF (5 mL) at RT. The reaction mixture was stirred for 1 h at RT, and then a solution of ethyl α-bromo-p-tolylacetate (1.0 g, 3.9 mmol) in anhydrous THF (5 mL) was added dropwise. After 12 h at RT, the solvent was removed in vacuo, and the residue was taken up in dichloromethane. The organic layers were washed with brine, dried, and evaporated. The residue was purified by chromatography (toluene) to give 0.46 g of the title compound as a colorless oil; IR (neat): 1734 cm−1; 1H NMR(CDCl3) d 1.16 (t, 3 H, J=7.0 Hz), 2.33 (s, 3 H), 4.13 (q, 2 H, J=7.0 Hz), 5.48 (s, 1H), 6.31 (m, 2 H), 6.95-7.40 (m, 10 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06806267B1 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-bfd4c08752d84ae98ddbca7d3cb91f42 |
| Source note | uspto-grants-2004_10 |