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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | tert-Butyl 3-(2-iodoethyl)azetidine-1-carboxylate | HCID 19034125 | — |
| Product | 3-[N-BOC-2-(Azetidin-3-yl)ethyl]-2-piperidone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05281585 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-9e40ad7eeb6d46dd809465c3dda55e9a |
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| Source note | uspto-grants-1994_01 |
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