HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095486Generated: October 30, 2026
Chlorotrimethylsilane → HCID 57475109, compound
https://huagongshe.com/reaction/1095486
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 8-(Dimethylamino)-1,4-dioxaspiro[4.5]decane-8-carbonitrile | HCID 360977 | — |
| Reactant | HCID 178505773 | HCID 178505773 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57475109 | HCID 57475109 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08138187B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-0a5a96ad2a474db5a8128824c0b98a88 |
|---|
| Source note | uspto-grants-2012_03 |
|---|