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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716019Generated: October 29, 2026

Hydrochloric Acid → HCID 86727233, compound

https://huagongshe.com/reaction/716019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant(5S)-5-(hydroxymethyl)-1,3-oxazolidin-2-oneHCID 2793787—
SolventDimethylformamideHCID 6228—
ProductHCID 86727233HCID 8672723374%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187495B2
Source datasetuspto-grants-2015_11
ORD IDord-75a75725c2114ddf87894d87d4a7416e
Source noteuspto-grants-2015_11