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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095477Generated: October 30, 2026

Chlorotrimethylsilane → HCID 57475095, compound

https://huagongshe.com/reaction/1095477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAmmonium ChlorideHCID 25517—
Reactant8-(Dimethylamino)-1,4-dioxaspiro[4.5]decane-8-carbonitrileHCID 360977—
ReactantHCID 178418336HCID 178418336—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57475095HCID 5747509552%

Reaction Steps

2 M benzylmagnesium chloride solution in THF (3, 285 ml, 570 mmol) was added to a solution of 8-dimethylamino-1,4-dioxa-spiro[4.5]decane-8-carbonitrile (39.8 g, 190 mmol) in THF (300 ml) in the course of 15 min, under argon and while cooling with ice. The mixture was then stirred at RT for 16 h. For working up of the reaction mixture, saturated ammonium chloride solution (200 ml) and water (100 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 then concentrated. A white solid (68.34 g) remained which, apart from the product, still contained the educt. The crude product was dissolved in ethyl methyl ketone (250 ml), and ClSiMe3 (30 ml, 238 mmol) was added, while cooling with ice. After 16 h, dimethyl-(8-benzyl-1,4-dioxa-spiro[4.5]dec-8-yl)amine hydrochloride was isolated in a yield of 52% (40.33 g) as a white solid with a melting point of 276-280° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138187B2
Source datasetuspto-grants-2012_03
ORD IDord-eeab108a6ff0452d9337fdfb7b13e0b4
Source noteuspto-grants-2012_03