HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690769Generated: October 30, 2026
Methyl iodide → 2,2-Dimethyl-1H-indene-1,3(2H)-dione
https://huagongshe.com/reaction/1690769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,3-Indandione | HCID 11815 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Product | 2,2-Dimethyl-1H-indene-1,3(2H)-dione | HCID 599983 | — |
Reaction Steps
Potassium fluoride on Celite® [loading wt: 50% purchased from Sigma-Aldrich Co.] (5.8 g, ˜50 mmol) is heated at 135° C. for 2 h under vacuum (<20 torr). The solid is then permitted to cool to room temperature and placed under a nitrogen atmosphere at which time a solution of indan-1,3-dione (CAS# 606-23-5, 1.46 g, 10.0 mmol) in acetonitrile (15 mL) is added followed by iodomethane (1.8 mL, 30 mmol). The reaction is heated in a sealed vessel at 70° C. overnight. The reaction mixture is cooled to room temperature and filtered through a pad of Celite®. The resulting residue is purified by silica gel flash chromatography (ethyl acetate-heptane, 0:1 to 1:9) to furnish 2,2-dimethyl-indan-1,3-dione; 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.30 (s, 6 H), 7.84-7.89 (m, 2 H), 7.96-8.02 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08153674B2 |
|---|
| Source dataset | uspto-grants-2012_04 |
|---|
| ORD ID | ord-23886fafeb4d46afa2cbc38fbf2f7fc1 |
|---|
| Source note | uspto-grants-2012_04 |
|---|