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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446088Generated: October 31, 2026

Triethyl phosphite → HCID 57758671, compound

https://huagongshe.com/reaction/446088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphiteHCID 31215—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 57758732HCID 57758732—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57758671HCID 5775867174.2%

Reaction Steps

To a solution of tert-butyl (3R)-3-methyl-5-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carboxylate (9.90 g, 32.6 mmol) and tri ethyl phosphite (6.71 mL, 39.1 mmol) in anhydrous tetrahydrofuran (165 mL), lithium bistrimethylsilyl amide (45.7 mL, 45.7 mmol, 1.0M solution in tetrahydrofuran) was added at −5° C., and the mixture was stirred at the same temperature for 30 minutes. After bubbling oxygen gas into the reaction mixture for 30 minutes, saturated aqueous solution of ammonium chloride (150 mL) was added in an ice bath, and the mixture was concentrated under reduced pressure. Water (100 mL) was added to the residue and the mixture was extracted with ethyl acetate (200 mL×2). The organic layer was washed with saturated aqueous solution of sodium chloride (200 mL), and dried with anhydrous sodium sulfate. After the filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate, 1:1→1:4) to obtain 7.73 g (74%) of the title compound as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476429B2
Source datasetuspto-grants-2013_07
ORD IDord-13c30a2d81aa4ef499f91a9f88b8a057
Source noteuspto-grants-2013_07