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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948602Generated: November 4, 2026

Chlorotrimethylsilane → HCID 57475109, compound

https://huagongshe.com/reaction/1948602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1-Bromo-3-fluorobenzeneHCID 14082—
ReactantAmmonium ChlorideHCID 25517—
Reactant8-(Dimethylamino)-1,4-dioxaspiro[4.5]decane-8-carbonitrileHCID 360977—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57475109HCID 57475109—

Reaction Steps

A solution of 1-bromo-3-fluorobenzene (5.00 g, 28.6 mmole) in absolute ether (15 ml) was added dropwise to a suspension of magnesium (694 mg, 28.6 mmole) in absolute ether (10 ml) at such a rate that the ether boiled. After completion of the addition the reaction mixture was stirred for 10 minutes at RT, following which the magnesium had completely dissolved. The reaction solution was cooled in an ice bath and 8-dimethylamino-1,4-dioxa-spiro[4.5]decane-8-carbonitrile (3.00 g, 14.3 mmole) in absolute THF (30 ml) was added dropwise at 10° C. The reaction mixture was stirred at room temperature overnight, 20% NH4Cl-solution (20 ml) and water (30 ml) were added thereto while cooling with ice, and the mixture was extracted with ether (3×50 ml). The organic phase was washed with water (50 ml) and then with saturated NaCl solution (50 ml), dried over Na2SO4 and concentrated by evaporation in vacuo. The crude product was dissolved in ethyl methyl ketone (25 ml), ClSiMe3 (3.2 ml, 25 mmole) was added while cooling with ice, and the mixture was stirred at room temperature for 5 hours. The precipitate formed was filtered off and dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399503B2
Source datasetuspto-grants-2013_03
ORD IDord-46a04ba79a9741adba37e662e56cfb3f
Source noteuspto-grants-2013_03