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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8756Generated: October 25, 2026

Propanal → tert-Butyl 4-(3-hydroxy-1-oxopent-1-yl)-4-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/8756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanalHCID 527—
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 4-acetyl-4-methoxypiperidine-1-carboxylateHCID 21983927—
ReactantLithium diisopropylamineHCID 45051747—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(3-hydroxy-1-oxopent-1-yl)-4-methoxypiperidine-1-carboxylateHCID 2198400455.9%

Reaction Steps

To a solution of tert-butyl 4-acetyl-4-methoxypiperidine-1-carboxylate (0.589 g, 2.29 mmol) from Step A in tetrahydrofuran (20 mL) at −78° C. was added lithium diisopropylamine (0.650 mL, 0.974 mmol) followed by propionaldehyde (0.266 g, 0.330 mL, 4.58 mmol). After 5 min, the reaction mixture was poured into saturated ammonium chloride, and extracted three times with diethyl ether. The organic layers were combined, washed with saturated sodium chloride solution, dried over sodium sulfite, filtered, and concentrated. The residue was purified by flash chromatography eluting with 40% ethyl acetate/hexanes to afford the title compound (0.404 g). MS/EI (acetonitrile/water): m/z 216.1 (M+1−BOC) retention time=2.69 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091211B2
Source datasetuspto-grants-2006_08
ORD IDord-b89820f3efd14138aa3a6cb136df92cc
Source noteuspto-grants-2006_08