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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365861Generated: November 1, 2026

Diethyl Ether → HCID 22872664, compound

https://huagongshe.com/reaction/365861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantHCID 22872671HCID 22872671—
ReactantHCID 178418255HCID 178418255—
ProductHCID 22872664HCID 22872664—

Reaction Steps

The 5-cyano-6-chloro-3-(1-BOC-2-(S)-azetidinylmethoxy)pyridine of example 92a in anhydrous Et2O at 0° C. is treated with 1.5 equivalents of phenylmagnesium bromide in Et2O and stirring is maintained at 0 to 35° C. until the nitrile is largely consumed. The solvent is evaporated and the residue is treated with 2M aqueous potassium hydrogen sulfate to hydrolyze the intermediate imine. The solution is made basic with potassium carbonate and extracted with EtOAc. The combined extracts are dried (Na2SO4) and concentrated to a residue which is chromatographed (silica gel) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127386
Source datasetuspto-grants-2000_10
ORD IDord-1f7694cf013542558486a93cffb25985
Source noteuspto-grants-2000_10