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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245576Generated: November 1, 2026

Ethyl ketone → HCID 18187644, compound

https://huagongshe.com/reaction/1245576

Reaction equation

Participants

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

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-(tert-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 the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125887B2
Source datasetuspto-grants-2006_10
ORD IDord-f73e1762ff004b2cbc08999eacb8658c
Source noteuspto-grants-2006_10