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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403448Generated: October 28, 2026

Chlorotrimethylsilane → HCID 86650528, compound

https://huagongshe.com/reaction/403448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant6-Chloropyridine-3-carbaldehydeHCID 2764053—
ReactantMagnesium ChlorideHCID 5360315—
ReactantHCID 57907447HCID 57907447—
SolventEthyl AcetateHCID 8857—
ProductHCID 86650528HCID 8665052888%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748433B2
Source datasetuspto-grants-2014_06
ORD IDord-fd349ef910ad4841bba622125d518a63
Source noteuspto-grants-2014_06