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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170740Generated: October 30, 2026

Carbonocyanidic acid, methyl ester → HCID 117665483, compound

https://huagongshe.com/reaction/2170740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonocyanidic acid, methyl esterHCID 28660—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 117665532HCID 117665532—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117665483HCID 11766548321%

Reaction Steps

A solution of lithium diisopropylamide (2.0 M in THF, 0.18 mL, 0.36 mmol) was added to a solution of 7-methoxy-4-(3-(trifluoromethyl)phenyl)-2,3-dihydro-1H-inden-1-one (103 mg, 0.34 mmol) in THF (1.1 mL) at −78° C. After 1 h at −78° C., methyl cyanoformate (40 μL, 0.50 mmol) was added and the reaction mixture was allowed to warm to room temperature. After stirring at room temperature overnight, the reaction was quenched with saturated aqueous NH4Cl (25 mL) and extracted with EtOAc (3×40 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated. The resulting crude residue was purified by combiflash (12 g column, hexanes→EtOAc, gradient) to afford 26 mg (21%) of methyl 7-methoxy-1-oxo-4-(3-(trifluoromethyl)phenyl)-2,3-dihydro-1H-indene-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051294B2
Source datasetuspto-grants-2015_06
ORD IDord-84f583893f38429cbf5b7f930c3178a8
Source noteuspto-grants-2015_06