HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → Methyl (3S)-3-(tert-butyldiphenylsilyloxy)-butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | Methyl 3-hydroxybutyrate, (S)- | HCID 6950307 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl (3S)-3-(tert-butyldiphenylsilyloxy)-butyrate | HCID 68783265 | — |
Reaction Steps
Methyl (S)-(+)-3-hydroxybutyrate (0.48 g, 4.04 mmol) (Aldrich) was dissolved in dichloromethane (6 mL, dried over molecular sieves). Imidazole (0.39 g, 5.65 mmol) (Aldrich) was added. When all had dissolved, tert-butyldiphenylsilyl chloride (1.05 mL, 4.04 mmol) was added dropwise and the mixture was stirred at room temperature for 4.5 hours. The reaction mixture was diluted with additional dichloromethane, washed with water (2×) and brine, dried over anhydrous sodium sulfate, filtered and concentrated. Purification by flash chromatography (Biotage 40M, 5:95 ethyl acetate-hexanes) gave (S)-3-(tert-butyl-diphenyl-silanyloxy)-butyric acid methyl ester. (Yield 1.33 g, 92.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115740B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-7318163c0f9a4655831e6d9de151afd2 |
| Source note | uspto-grants-2006_10 |