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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862709Generated: October 31, 2026

Ethyl ketone → HCID 18187644, compound

https://huagongshe.com/reaction/1862709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ketoneHCID 7288—
ReactantDiisopropylamineHCID 7912—
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18187644HCID 1818764485%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of diisopropylamine (0.63 mL, 4.5 mmol) in THF (16 mL) at 0° C. was treated with 1.6 M n-butyllithium in sol'n in hexanes (2.8 mL). The resulting solution was stirred at 0° C. for 10 min, then cooled to −78° C. 3-Pentanone (0.41 mL, 4.1 mmol) was added and the resulting mixture was stirred cold for 1 h. A solution of 1-(t-butoxycarbonyl)-4-formylpiperidine (435 mg, 2.05 mmol) (from Step B) in THF (3 mL) was then added. After 15 min, the reaction was quenched with sat'd ammonium chloride (25 mL) and extracted with ether (100 mL). The extract was dried over magnesium sulfate and concentrated. MPLC (Biotage) on a 40S silica cartridge using 4:1 v/v, then 3:2 v/v hexanes/ethyl acetate as the eluent afforded 517 mg (85%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06538002B1
Source datasetuspto-grants-2003_03
ORD IDord-0c21676921344ab4acaa249cdb294c51
Source noteuspto-grants-2003_03