HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403448Generated: October 28, 2026
Chlorotrimethylsilane → HCID 86650528, compound
https://huagongshe.com/reaction/403448
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Chloropyridine-3-carbaldehyde | HCID 2764053 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Reactant | HCID 57907447 | HCID 57907447 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86650528 | HCID 86650528 | 88% |
Reaction Steps
To a stirred solution of 23.0 g (837 mmol) of (4S)-4-benzyl-3-hex-5-ynoyl-1,3-oxazolidin-2-one from step A above in 200 mL of anhydrous ethyl acetate at ambient temperature under an atmosphere of nitrogen was added 1.6 g (17 mmol) of anhydrous magnesium chloride, 23.0 mL (166 mmol) of triethylamine, 14.0 g (100 mmol) of 6-chloropyridine-3-carboxaldehyde and 16.0 mL (124 mmol) of chlorotrimethylsilane and the resulting mixture was stirred for 72 h. The heterogeneous reaction mixture was filtered through a 300 mL plug of silica gel eluting with an additional 1 L of ethyl acetate. The filtrate was evaporated to dryness in vacuo and the residue suspended in 200 mL of methanol and 5.0 mL of trifluoroacetic acid. The resulting mixture was stirred at ambient temperature under nitrogen for 5 hours during which time the reaction became homogeneous. All volatiles were then removed in vacuo and the residue was purified by silica gel chromatography eluting with a 10-15% ethyl acetate in hexanes gradient to afford the title compound as a white solid (30 g, 88%). LC-MS: m/z (ES) 413.2 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748433B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-fd349ef910ad4841bba622125d518a63 |
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| Source note | uspto-grants-2014_06 |
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