HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901205Generated: October 30, 2026
Imidazole → ethyl (R)-alpha-(t-butyldimethylsilyloxy)-alpha-phenylacetate
https://huagongshe.com/reaction/1901205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (-)-Ethyl mandelate | HCID 6951556 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl (R)-alpha-(t-butyldimethylsilyloxy)-alpha-phenylacetate | HCID 53734821 | — |
Reaction Steps
A solution of 31.4 g of t-butyldimethylsilyl chloride in 200 ml of dimethylformamide was added dropwise to a solution of 25 g of ethyl (R)-(-)-mandelate and 28.4 g of imidazole in 600 ml of anhydrous dimethylformamide, and the resulting mixture was stirred overnight at 40° C. The dimethylformamide solvent was then removed by distillation under reduced pressure, and the residue was mixed with water and then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was then removed by distillation under reduced pressure. The resulting residue was purified by column chromatography through silica gel, using a 1:10 by volume mixture of ethyl acetate and hexane as the eluent. The title compound was obtained as a liquid, boiling at 129° C./3.5 mmHg (466 Pa) by distillation in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05576340 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-9f1b5efd81c34e09a0c6950347b0e3af |
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| Source note | uspto-grants-1996_11 |
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