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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669743Generated: October 30, 2026

Tetrahydrofuran → HCID 59865005, compound

https://huagongshe.com/reaction/1669743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 2-oxopiperidine-1-carboxylateHCID 7577838—
ReactantHCID 59865001HCID 59865001—
ReactantHCID 178418918HCID 178418918—
SolventEthyl AcetateHCID 8857—
ProductHCID 59865005HCID 59865005—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A solution of 1-{3-[(4-iodophenyl)oxy]propyl}-3,3-dimethylpiperidine (25 g) in THF (125 ml) is stirred for about 15 min, then cooled to 0-5° C. Isopropyl magnesium chloride solution (70.5 ml, 1.9M) is added at 0-5° C. over about 40 min, then the mixture is stirred at 0-5° C. for 2-3 h. The mixture is then cooled to −78 to −80° C. and a precooled solution (−20 to −30° C.) of N-Boc-piperidinone (16 g) in THF (125 ml) is added over about 1-2 h and the reaction mixture is stirred for about 1.5 h at −78 to −80° C. The reaction mixture is allowed to warm to 25-30° C., then stirred for 23-24 h. Saturated ammonium chloride solution (375 ml) is added at 25-30° C., followed by ethyl acetate (500 ml) and the mixture stirred for about 50 min. The aqueous layer is extracted with ethyl acetate (250 ml). The combined organic layers are washed with water (375 ml), dried over sodium sulfate and concentrated under reduced pressure to give the crude title compound (30.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989629B2
Source datasetuspto-grants-2011_08
ORD IDord-50fc68c6c393496ea348f08e7362dd7d
Source noteuspto-grants-2011_08