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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199372Generated: October 29, 2026

1-Indanone → HCID 11435017, compound

https://huagongshe.com/reaction/2199372

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IndanoneHCID 6735—
ReactantAmmonium ChlorideHCID 25517—
Reactant2,2,2-Trifluoroethyl trifluoroacetateHCID 67888—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11435017HCID 1143501798%

Reaction Steps

To a 0° C. solution of LiHMDS (0.65 mL, 0.6 M in THF) was added a solution of 1-indanone (26 mg, 0.19 mmol) in THF (1.0 mL). The reaction mixture was allowed to warm to room temperature over 20 min, and then CF3CO2CH2CF3 was added (55 μL, 0.41 mmol). After an additional 20 min at room temperature, saturated aqueous NH4Cl (5 mL) was added, and the resulting mixture was extracted with EtOAc (3×5 mL). The organics were dried over Na2SO4 and concentrated under reduced pressure. Without purification, the crude mixture was immediately subjected to general procedure B. SiO2 flash chromatography (25% EtOAc in hexanes) afforded the 2-methlyene-1-indanone as a yellow oil (28 mg) in 98% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359277B2
Source datasetuspto-grants-2016_06
ORD IDord-7cb5cab4434c4513a88e8801a7e8380e
Source noteuspto-grants-2016_06