HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110116Generated: October 31, 2026
Methyl iodide → Methyl 2-methyl-2,3-dihydro-1H-indene-2-carboxylate
https://huagongshe.com/reaction/2110116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Methyl indane-2-carboxylate | HCID 9964238 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-methyl-2,3-dihydro-1H-indene-2-carboxylate | HCID 57565328 | 9% |
Reaction Steps
Indane-2-carboxylic acid methyl ester (550 mg, 3.125 mmol) was dissolved in THF (20 mL). At −78° C. LiHMDS (1M solution in THF, 3.75 mL) was added into the reaction mixture. The solution was stirred for 15 min at −78° C., warmed to 0° C. for 15 min and then −78° C. for an additional 15 min. Methyl iodide (250 μL, 4.01 mmol) was then added into the reaction mixture followed by stirring at −78° C. for 15 min, room temperature for 30 min and then quenched with saturated ammonium chloride. The solution was then diluted with diethyl ether and washed with saturated sodium bicarbonate, brine, dried (MgSO4), filtered and concentrated. The crude mixture was then purified by silica gel flash column chromatography to afford 2-methyl-indan-2-carboxylic acid methyl ester (52 mg, 9%) as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.16 (m, 4H), 3.72 (t, 3H), 3.48 (d, 2H), 2.81 (d, 2H), 1.36 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517884B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-bd390d656de749c2ac4c16a78a95e57d |
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| Source note | uspto-grants-2009_04 |
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