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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbonocyanidic acid, methyl ester | HCID 28660 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 117665532 | HCID 117665532 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117665483 | HCID 117665483 | 21% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051294B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-84f583893f38429cbf5b7f930c3178a8 |
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| Source note | uspto-grants-2015_06 |
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