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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355432Generated: October 29, 2026

Chlorotrimethylsilane → HCID 59383072, compound

https://huagongshe.com/reaction/2355432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantLithium diisopropylamideHCID 2724682—
Reactant4-Bromobenzo[b]thiopheneHCID 12094208—
ReactantTetrahydrofuran heptaneHCID 21263495—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59383072HCID 59383072—

Reaction Conditions

Temperature-70 °C

Reaction Steps

A stirred solution of ˜80% pure 4-bromobenzothiophene (580 mg, 2.7 mmol) and chlorotrimethylsilane (0.70 mL, 5.4 mmol) in dry THF (10 mL) was cooled to −70° C. and 2 M LDA in 1:1 THF/heptane (1.35 mL, 5.4 mmol) was added dropwise over 2 min. The mixture was stirred at −70° C. for 1.5 h and diluted with ether (80 mL) and 5% aq HCl (20 mL). The organic layer was separated, washed with sat'd aq NaHCO3 (20 mL) and dried over MgSO4. Removal of the solvent left 4-bromo-2-(trimethylsilyl)benzothiophene (740 mg, 95%) as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-b207a1bed93c40cbadfb68ab494c0cd9
Source noteuspto-grants-2010_07