HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716019Generated: October 29, 2026
Hydrochloric Acid → HCID 86727233, compound
https://huagongshe.com/reaction/716019
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | (5S)-5-(hydroxymethyl)-1,3-oxazolidin-2-one | HCID 2793787 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86727233 | HCID 86727233 | 74% |
Reaction Steps
(S)-5-(hydroxymethyl)oxazolidin-2-one (570 mg, 4.87 mmol, as described by Danielmeier, K.; Steckhan, E. Tet. Asymmetry, 6(5), 1995, 1181) and imidazole (331 mg, 4.87 mmol) were dissolved in dimethylformamide (5 mL) and cooled to 0° C. tert-Butylchlorodiphenylsilane (1.34 g, 4.87 mmol) was added dropwise at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 5 hours. The mixture was was poured into 0.5 N HCl (50 ml), and the resultant mixture was extracted with ethyl acetate. The layers were separated, and the organic phase was washed with saturated sodium bicarbonate, water and brine. The organic phase was dried over sodium sulfate and the solvent removed to afford crude material that was purified on a silica gel column (50% ethyl acetate in hexanes) to give the title compound (1.28 g, 74.0%). 1H NMR (300 MHz, DMSO-d6) δ: 1.0 (s, 9 H) 3.3-3.6 (m, 2 H) 3.6-3.9 (m, 2 H) 4.6-4.8 (m, 1 H) 7.3-7.8 (m, 11 H). MS (ES) (M+23)+: 278 for the Na+ adduct of C20H25NO3Si.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187495B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-75a75725c2114ddf87894d87d4a7416e |
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| Source note | uspto-grants-2015_11 |
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