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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantMethyl AcrylateHCID 7294—
ReactantTesmilifene HydrochlorideHCID 175534—
Reactant2-Iodo-4,5-dimethoxybenzaldehydeHCID 11011763—
CatalystZincHCID 23994—
SolventWaterHCID 962—
Productmethyl 5,6-dimethoxy-1H-indene-2-carboxylateHCID 1242347221.3%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062076B2
Source datasetuspto-grants-2015_06
ORD IDord-14bd130193fc4188902ee66da0fcd1c8
Source noteuspto-grants-2015_06