HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381500Generated: October 31, 2026
Tetrahydrofuran → 1-(4-fluorobenzyl)-5-phenyl-1H-pyrrole-2-carboxylic acid methoxy-methylamide
https://huagongshe.com/reaction/381500
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluorobenzyl bromide | HCID 68021 | — |
| Reactant | 5-phenyl-1H-pyrrole-2-carboxylic acid methoxymethylamide | HCID 54409440 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(4-fluorobenzyl)-5-phenyl-1H-pyrrole-2-carboxylic acid methoxy-methylamide | HCID 20696804 | — |
Reaction Steps
To a 100 mL round bottomed flask containing 5-phenyl-1H-pyrrole-2-carboxylic acid methoxymethylamide AV-6-1 (0.692 g, 3.01 mmol) was added a stirring bar and an argon inlet was attached. THF (15 mL) was added and, when all of the solids had dissolved, NaH-oil suspension (0.132 g of a 60% w/w suspension, 3.31 mmol) was added. This mixture was stirred 15 min at ambient temperature then 4-fluorobenzylbromide (0.41 mL, 3.31 mmol) was added. The resulting mixture was stirred 24 h at ambient temperature. The mixture was diluted with EtOAc and the solution was washed with 1N HCl, water and brine. Drying (MgSO4), filtration and removal of the solvent in vacuo gave an oil. This material was chromatographed on silica gel using 25% EtOAc in hexanes a eluant to give 1-(4-fluorobenzyl)-5-phenyl-1H-pyrrole-2-carboxylic acid methoxy-methyl-amide AV-7-1. 1H NMR (CDCl3) δ 3.21 (3H, s), 3.47 (3H, s), 5.52 (2H, s), 6.24 (1H, d, j=3.9 Hz), 6.75 to 6.90 (5H, m), 6.94 (1H, d, j=3.9 Hz), 7.38 (4H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06306891B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-7b8418e229524a65954b599ae113f6d1 |
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| Source note | uspto-grants-2001_10 |
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