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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879923Generated: November 3, 2026

Isobutyl iodide → HCID 59327423, compound

https://huagongshe.com/reaction/1879923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl iodideHCID 10556—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylateHCID 2758812—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 59327423HCID 5932742384%

Reaction Conditions

Temperature-5 °C

Reaction Steps

4.7 g (47 mmol) DIPEA in THF at −5° C. was treated slowly with 29.1 mL (47 mmol) n-Buli (1.6N in hexane) and stirred for 30 min at −5° C. and subsequently cooled to −75° C. and stirred for 2 h. A solution of 10 g (39 mmol) ethyl 1-tert-butoxycarbonylpiperidine-4-carboxylate (commercially available) in THF was added and the mixture was stirred for 2 h at −75° C. 8.51 g (47 mmol) 1-iodo-2-methylpropane was added and the mixture was allowed to stir to room temperature over night. The mixture was quenched at 0° C. with citric acid 10% aq. and extracted with ethyl acetate. The combined organic layers were washed with NaCl aq. sat., dried with Na2SO4, filtered and evaporated. The residue was purified by column chromatography on silica eluting with a gradient formed heptane and t-butyl-methylether. The combined product fractions were evaporated to yield 10.2 g (84%) of the title compound as light yellow oil. MS (m/e): 331.2 (M+NH4+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318749B2
Source datasetuspto-grants-2012_11
ORD IDord-4aaa46bf10a240dfa0843b0981be0379
Source noteuspto-grants-2012_11