HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422220Generated: October 30, 2026
Tetrahydrofuran → HCID 16639026, compound
https://huagongshe.com/reaction/422220
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Methoxyindan-1-one | HCID 78787 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 16639026 | HCID 16639026 | 67% |
Reaction Steps
Combine NaH (5.4 g, 122.1 mmol), THF anhydrous (150 mL), and dimethylcarbonate (6.6 mL, 81.3 mmol). While refluxing the reaction under a nitrogen atmosphere, add dropwise 5-Methoxyindanone (3.46 g, 21.33 mmol) over one hour. After the reaction mixture refluxes for 12 hours, quench using Acetic acid and then add Ethyl acetate to the reaction mixture in a separatory funnel. Wash the organic layer several times with water and dry the organic layer over Na2SO4 followed by concentration under reduced pressure. Flash Chromatograph using 1:1 Hexanes:Ethyl acetate to afford 3.14 g, 14.3 mmol (67% yield) of the title compound: 1H NMR (500 MHz, CDCl3); 3.3-3.4 (1H, dd), 3.5-3.6 (1H, dd), 3.7-3.8 (1H, m), 3.8 (3H, s), 3.9 (3H, s), 6.8-7.0 (2H, m), 7.7-7.8 (1H, m); TLC 2:1 Hexanes:Ethyl acetate Rf:=0.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08101638B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-1870dd6ffe18498e8d433cfa703e1744 |
|---|
| Source note | uspto-grants-2012_01 |
|---|