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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095486Generated: October 30, 2026

Chlorotrimethylsilane → HCID 57475109, compound

https://huagongshe.com/reaction/1095486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAmmonium ChlorideHCID 25517—
Reactant8-(Dimethylamino)-1,4-dioxaspiro[4.5]decane-8-carbonitrileHCID 360977—
ReactantHCID 178505773HCID 178505773—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57475109HCID 5747510955%

Reaction Steps

0.5 M 3-fluorophenylmagnesium bromide solution in THF (3, 750 ml, 375 mmol) was added to a solution of 8-dimethylamino-1,4-dioxa-spiro[4.5]decane-8-carbonitrile (19.8 g, 94 mmol) in THF (100 ml) in the course of 15 min, under argon and while cooling with ice, and the mixture was then stirred at room temperature for 16 h. For working up of the reaction mixture, saturated ammonium chloride solution (150 ml) and water (60 ml) was added, while cooling with ice, and the mixture was extracted with diethyl ether (3×100 ml). The organic phase was extracted by shaking with water (50 ml) and saturated NaCl solution (50 ml) and the extract was concentrated. A brown oil (26.5 g) remained which, apart from the phenyl compound 4, still contained the ketal 2. The crude product was dissolved in ethyl methyl ketone (156 ml), and ClSiMe3 (17.8 ml, 141 mmol) was added, while cooling with ice. After a reaction time of 6 h, it was possible to isolate the hydrochloride in a yield of 55% (16.3 g) as a white solid with a melting point of 275-278° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138187B2
Source datasetuspto-grants-2012_03
ORD IDord-0a5a96ad2a474db5a8128824c0b98a88
Source noteuspto-grants-2012_03