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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513099Generated: October 27, 2026

Diiodomethane → 1-Tert-butyl 3-ethyl 3-(iodomethyl)piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/513099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantDiisopropylamineHCID 7912—
Reactantn-Butyl lithiumHCID 61028—
Reactant1-Tert-butyl 3-ethyl piperidine-1,3-dicarboxylateHCID 357727—
SolventTetrahydrofuranHCID 8028—
Product1-Tert-butyl 3-ethyl 3-(iodomethyl)piperidine-1,3-dicarboxylateHCID 6831493277.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of diisopropylamine (14.6 mmol, 2.05 mL) in THF (15 mL) was cooled to −78° C. N-butyllithium (1.6 M in hexane) (16 mmol, 10 ml) was added dropwise and the solution was stirred for 30 minutes at 0° C. After cooling to −78° C. a solution of 1-tert-butyl 3-ethyl piperidine-1,3-dicarboxylate (14.6 mmol, 3.75 g) in 20 ml THF was added and the solution was stirred for 3 h at −78° C. A solution of diiodomethane (16 mmol, 1.3 mL) in THF (10 mL) was added and the solution was stirred for 2 days at room temperature. The reaction was quenched by the addition of water and extracted twice with EtOAc. The organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The crude was purified by flash chromatography (heptane/EtOAc: 10 to 50%) yielding the title compound (C1) (4.5 g, 74%). MS (ES) C14H24INO4 requires: 397. found: 420.1 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102676B2
Source datasetuspto-grants-2015_08
ORD IDord-2cd957f2209c49718a508244bff04d93
Source noteuspto-grants-2015_08