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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614052Generated: November 1, 2026

Chlorotrimethylsilane → HCID 86746649, compound

https://huagongshe.com/reaction/1614052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86746650HCID 86746650—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventAcetonitrileHCID 6342—
ProductHCID 86746649HCID 86746649—

Reaction Steps

Mix trifluoroacetic acid (30 mL) with acetonitrile (10 mL) and add, by dropwise addition, to an ice-cold solution of N-(9-phenylfluorenyl)-3(R)-[(diethoxyphosphinyl)acetyl]piperidine-2(R)-carboxylic acid, tert-butyl ester (3.5 g, 5.8 mmol) in acetonitrile (40 mL) and water (4 mL). Stir for 15 minutes, warm to room temperature and stir for an additional hour. Pour into saturated aqueous sodium hydrogen carbonate (500 mL) and extract into ethyl acetate (3×200 mL). Evaporate to a residue and take up the residue in acetonitrile (20 mL) and methylene chloride (20 mL). Place under a nitrogen atmosphere and add trimethylsilyl chloride (5 mL, 35 mmol). Stir overnight then add water. Stir for 15 minutes then blow to a residue with a stream of dry nitrogen. Take up the residue in water (100 mL) and wash with toluene (5×100 mL). Freeze dry to give a residue. Take up the residue in methanol (10 mL) and isopropanol (5 mL). Add propylene oxide (5 mL) and filter to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194430
Source datasetuspto-grants-1993_03
ORD IDord-e68f5aebd2db4930bd8015e70df49af6
Source noteuspto-grants-1993_03