HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82829Generated: October 28, 2026
Nitrogen → 5-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]-2-(methoxymethyl)thiazole
https://huagongshe.com/reaction/82829
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | (5-(((Tert-butyldimethylsilyl)oxy)methyl)thiazol-2-yl)methanol | HCID 86698207 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]-2-(methoxymethyl)thiazole | HCID 86698206 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of (5-(((tert-butyldimethylsilyl)oxy)methyl)thiazol-2-yl)methanol (1.21 g, 4.65 mmol) in CH2Cl2 (3.0 mL) was treated with MeI (0.35 mL, 5.57 mmol) followed by Ag2O (1.61 g, 6.97 mmol) and the resulting mixture (protected from light) was stirred overnight at 40° C. The reaction mixture was filtered and the solvent was removed under reduced pressure. Purification of the residue by FC (4:1 hept-EA) gave the title compound as a yellow oil: TLC: rf (4:1 hept-EA)=0.27. LC-MS-conditions 07: tR=0.99 min, [M+H]+=273.95.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846733B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-e487a37633ba4dbbbc5fd65b22b1ce20 |
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| Source note | uspto-grants-2014_09 |
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