Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095481Generated: October 27, 2026

Chlorotrimethylsilane → HCID 57475102, compound

https://huagongshe.com/reaction/1095481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant8-(1-Pyrrolidinyl)-1,4-dioxaspiro[4.5]decane-8-carbonitrileHCID 360976—
ReactantHCID 178478979HCID 178478979—
ProductHCID 57475102HCID 5747510243%

Reaction Steps

8-Pyrrolidin-1-yl-1,4-dioxaspiro[4.5]decane-8-carbonitrile (10.0 g, 42.6 mmol), dissolved in THF (90 ml), was added to a 1.82 M phenylmagnesium chloride solution in THF (70 ml, 0.127 mol) in the course of 15 min, under argon and while cooling with ice, and the mixture was stirred at room temperature for 16 h. For working up of the reaction mixture, saturated ammonium chloride solution (100 ml) was added, while cooling with ice, and the mixture was then extracted with diethyl ether (3×100 ml). The organic phase was extracted by shaking with water (70 ml) and saturated NaCl solution (70 ml) and the extract was concentrated. A yellow crystal slurry (11.8 g) remained which, apart from the desired product, still contained educt. The crude product was dissolved in ethyl methyl ketone (70 ml), and ClSiMe3 (8 ml, 0.063 mol) was added, while cooling with ice. After a reaction time of 6 h, it was possible to isolate 4-(8-phenyl-1,4-dioxaspiro[4.5]dec-8-yl)pyrrolidine hydrochloride in a yield of 43% (5.9 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138187B2
Source datasetuspto-grants-2012_03
ORD IDord-1a9b317cddd044d6b5bb84e8122a6acb
Source noteuspto-grants-2012_03