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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384380Generated: October 30, 2026

Triethylsilane → 5-Bromo-2,2-dimethyl-2,3-dihydro-1H-indene

https://huagongshe.com/reaction/384380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
Reactant6-Bromo-2,2-dimethyl-2,3-dihydro-1H-inden-1-oneHCID 20082014—
SolventTrifluoroacetic acidHCID 6422—
Product5-Bromo-2,2-dimethyl-2,3-dihydro-1H-indeneHCID 14838844205.2%

Reaction Steps

6-Bromo-2,2-dimethyl-indan-1-one 45a (7.23 g, 30.3 mmol) was dissolved in 150 mL of trifluoroacetic acid followed by addition of triethylsilane (12.1 mL, 75.6 mmol). The reaction mixture was stirred overnight at room temperature. The reaction was monitored by TLC until the disappearance of the starting materials and then quenched by addition of water. The mixture was concentrated under reduced pressure to remove trifluoroacetic acid. The mixture was adjusted to be basic with saturated aqueous sodium bicarbonate and then extracted with ethyl acetate (50 mL×3). The combined organic extracts were washed with saturated brine, dried over anhydrous sodium sulfate, filtered to remove the drying agent and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound 5-bromo-2,2-dimethyl-indan 45b (14 g) as a colourless oil, which was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-733bb4b8f8bd4bf99c3d20d24ccdc63a
Source noteuspto-grants-2013_02