HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175693Generated: October 26, 2026
Acetonitrile → methyl 5,6-dimethoxy-1H-indene-2-carboxylate
https://huagongshe.com/reaction/2175693
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | Tesmilifene Hydrochloride | HCID 175534 | — |
| Reactant | 2-Iodo-4,5-dimethoxybenzaldehyde | HCID 11011763 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Product | methyl 5,6-dimethoxy-1H-indene-2-carboxylate | HCID 12423472 | 21.3% |
Reaction Steps
2-Iodo-4,5-dimethoxybenzaldehyde (292 mg, 1.0 mmol), CoCl2 (dppe) complex (26.4 mg, 0.05 mmol), dppe (19.9 mg, 0.05 mmol) and zinc power (179.8 mg, 2.75 mmol) were placed in a vial, which was sealed with a septum and flushed several times with nitrogen. Acetonitrile (3 mL) and methyl acrylate (172 mg, 2.0 mmol) were then sequentially added and the mixture was heated at 80° C. overnight. Water was then added and the mixture was extracted with ethyl acetate. The organic extracts were concentrated under reduced pressure and the residue was purified by flash chromatography using petroleum ether/ethyl acetate 8:1 (v:v) as eluent to give methyl 5,6-dimethoxy-1H-indene-2-carboxylate (50 mg, 21%). LC-MS (ES-API); rt 7.89 min; m/z calculated for C13H14O4 [M+H]+ 235.1, found 235.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062076B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-14bd130193fc4188902ee66da0fcd1c8 |
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| Source note | uspto-grants-2015_06 |
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