HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221629Generated: October 31, 2026
Bromotrimethylsilane → [5-(Tert-butyldiphenylsilyloxymethyl)-2-phenyl-1,3-oxazol-4-yl]methanol
https://huagongshe.com/reaction/2221629
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Tert-butyldiphenylsilyloxymethyl-4-methoxymethoxymethyl-2-phenyl-1,3-oxazole | HCID 11488680 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | [5-(Tert-butyldiphenylsilyloxymethyl)-2-phenyl-1,3-oxazol-4-yl]methanol | HCID 11189974 | — |
Reaction Steps
To a mixture of 5-tert-butyldiphenylsilyloxymethyl-4-methoxymethoxymethyl-2-phenyl-1,3-oxazole (20.0 g) and chloroform (250 mL) added dropwise trimethylsilyl bromide (25.0 g) at −40° C. The reaction mixture was stirred at −40° C. for 30 min, and the mixture was further stirred at room temperature for 1 hr. The reaction mixture was poured into saturated aqueous sodium hydrogen carbonate, and extracted with chloroform. The organic layer was dried over magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography and eluted with ethyl acetate-hexane (1:2, v/v) to give [5-(tert-butyldiphenylsilyloxymethyl)-2-phenyl-1,3-oxazol-4-yl]methanol. Recrystallization from hexane-ethyl acetate gave colorless crystals (10.2 g, yield 56%). melting point: 95-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07368578B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-35551a6a8c6b41a39e3e5918033e8db4 |
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| Source note | uspto-grants-2008_05 |
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