HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852781Generated: October 31, 2026
Chlorotrimethylsilane → HCID 178429767, compound
https://huagongshe.com/reaction/852781
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 5-(Trifluoromethyl)dibenzothiophen-5-ium-3-sulfonate | HCID 2777499 | — |
| Reactant | HCID 178435098 | HCID 178435098 | — |
| Product | HCID 178429767 | HCID 178429767 | — |
Reaction Steps
A dry 100 mL round-bottomed flask equipped with a magnetic stir bar under an atmosphere of N2 was charged with 528 mg (2.35 mmol) of 2-(bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one in 5 mL of anhydrous THF. The reaction was cooled to −20° C. and 5.0 mL (5.0 mmol) of NaHMDS (11.0M in THF) were added drop-wise via syringe. The resulting reaction mixture was stirred at −20° C. for 30 min then 0.86 mL (6.78 mmol) of TMSCl was added drop-wise via syringe. The reaction mixture was held at −20° C. for 15 min, and then the mixture was allowed to warm to ambient temperature. After stirring the reaction mixture for an additional 1 h, the mixture was concentrated in vacuo. The reaction flask was again equipped with a magnetic stir bar and placed under an N2 atmosphere. Anhydrous CH3CN was added, and 978 mg (2.58 mmol) of S-(trifluoromethyl)dibenzothiophenium-3-sulfonate C2 H5OH was added to the reaction mixture in one portion, and the resulting suspension was stirred at ambient temperature for 19 h. The solids were then removed by filtration through a Celite pad, and the reaction flask and pad were rinsed with CH2Cl2. The organic layer was washed with 20 mL of 1:1 H2O/sat'd NH4Cl, and the aqueous layer was extracted with an additional portion of CH2Cl2. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. Flash chromatography (SiO2, CH2Cl2 to 5% MeOH/CH2Cl2) provided the desired compound. MS (ESI, pos. ion) m/z: 293.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253196B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-9adb0540f2d64a4e93a00007c768e2f0 |
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| Source note | uspto-grants-2007_08 |
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