HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (R)-1-t-Butyldimethylsilyloxy-3-hydroxytetradecane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | HCID 11791041 | HCID 11791041 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-1-t-Butyldimethylsilyloxy-3-hydroxytetradecane | HCID 54036929 | 84% |
Reaction Steps
To a solution of diol compound 9 (2.28 g, 10 mmol) in N,N-dimethyl formamide (50 mL) at 0° C. was added sequentially imidazole (1.63 g, 24 mmol), and t-butyldimethylsilyl chloride (1.65 g, 11 mmol), and the reaction mixture was stirred for 2 h. After completion of the reaction (TLC). The mixture was diluted with ethyl acetate (200 mL), washed with water (2×50 mL), dried and concentrated to give a colorless oil, which after purification by flash chromatography, afforded the pure monosilyl compound 10 as an oil (Rf 0.71, silica, ethyl acetate and hexane, 1:10, 2.80 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05593969 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-bc2ddfe645b94e6f904d6b2291cf7347 |
| Source note | uspto-grants-1997_01 |