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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084552Generated: October 30, 2026

Bromotrimethylsilane → 1,5-Dibromo-2,3-dihydro-1H-indene

https://huagongshe.com/reaction/2084552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrimethylsilaneHCID 76113—
Reactant5-bromo-2,3-dihydro-1H-inden-1-olHCID 13486299—
SolventChloroformHCID 6212—
Product1,5-Dibromo-2,3-dihydro-1H-indeneHCID 22732572—

Reaction Steps

The compound obtained in Step A (70.19 mmol) is brought into solution in 420 ml of CHCl3, and bromotrimethylsilane (13.90 ml, 105.28 mmol, 1.5 eq.) is added at room temperature. The reaction mixture is stirred overnight at room temperature. The solvent and excess bromotrimethylsilane are removed by evaporation under reduced pressure. The oil is taken up in 150 ml of CHCl3, washed with 2×80 ml of water and 3×100 ml of saturated NaCl and dried over Na2SO4. The organic phase is then concentrated under reduced pressure to yield the title compound in the form of a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716852B2
Source datasetuspto-grants-2004_04
ORD IDord-20974b9e15294dafbc8e34a64e6b255b
Source noteuspto-grants-2004_04