HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977987Generated: October 31, 2026
Water → (6-Methoxyindan-1-ylidene) acetonitrile
https://huagongshe.com/reaction/1977987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| Reactant | 6-Methoxy-1-Indanone | HCID 334036 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-Methoxyindan-1-ylidene) acetonitrile | HCID 53954914 | 53% |
Reaction Steps
To a solution of 60% sodium hydride (2.71 g, 67.9 mmol) in THF (150 ml) was added dropwise, under ice-cooling, diethyl cyanomethylphosphonate (11.5 g, 64.8 mmol). The mixture was stirred for 15 hours, to which was then added dropwise a solution of 6-methoxy-1-indanone (10.0 g, 61.7 mmol) in THF (30 ml). The reaction mixture was stirred for 30 minutes at room temperature. The reaction mixture was poured into water, and the organic layer was subjected to extraction with ethyl acetate. The extract solution was washed with brine and water, followed by drying over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (hexane:ethyl acetate=8:2). Recrystallization of the product-from ethyl acetate/hexane afforded the above-titled compound (6.00 g, yield 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06235789B1 |
|---|
| Source dataset | uspto-grants-2001_05 |
|---|
| ORD ID | ord-92130f1b6f304db881c45fd69cf1ccb9 |
|---|
| Source note | uspto-grants-2001_05 |
|---|