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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198504Generated: November 2, 2026

Tetrahydrofuran → 3-[N-BOC-2-(Azetidin-3-yl)ethyl]-2-piperidone

https://huagongshe.com/reaction/1198504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLithium diisopropylamideHCID 2724682—
Reactanttert-Butyl 3-(2-iodoethyl)azetidine-1-carboxylateHCID 19034125—
Product3-[N-BOC-2-(Azetidin-3-yl)ethyl]-2-piperidoneHCID 19380936—

Reaction Steps

A solution of 135 (for preparation see; D. H. Hua, et. al., JOC, 55, 3682, 1990) (0.19 g, 1.2 mmol) in THF (3.9 mL) at -78° C. was added LDA (0.58 mL, 1.2 mmol, 2.0M/heptane/THF/ethylbenzene) dropwise. After 15 min 134 (0.30 g, 0.96 mmol) in THF (3.5 mL) was added dropwise. After stirring 1.0 h, the reaction was quenched with CH3OH (7.5 mL) and the resulting solution warmed to ambient temperature. The solution was then diluted with EtOAc and then washed with H2O, 5% KHSO4, sat. NaHCO3, and brine, dried (MgSO4), and concentrated to give 136 (0.27 g) as a white solid. Rf 0.25 (silica, 2:1 CH2Cl2 /acetone). 1H ITMR (400 MHz, CDCl3) δ 5.81 (bs, 1H), 3.95 (m, 2H), 3.54 (m, 2H), 3.10 (m, 2H), 2.47 (m, 1H), 2.26 (m, 1H), 2.00-1.40 (m, 8H), 1.43 (s, 9H). ##STR60##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281585
Source datasetuspto-grants-1994_01
ORD IDord-9e40ad7eeb6d46dd809465c3dda55e9a
Source noteuspto-grants-1994_01