Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245601Generated: November 1, 2026

Acetaldehyde → HCID 21912733, compound

https://huagongshe.com/reaction/1245601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantDiisopropylamineHCID 7912—
ReactantEthyl 1-((1,1-dimethylethoxy)carbonyl)-4-piperidineacetateHCID 9993342—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21912733HCID 21912733—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 0.35 mL (2.5 mmol) of diisopropylamine in 10 mL of THF at 0° C. was treated with 1.6 mL of 1.0 M n-butyllithium solution in hexanes. The resulting mixture was stirred at 0° C. for 10 min, then cooled to −78° C. A solution of 540 mg (2.0 mmol) of ethyl 2-(1-tert-butoxycarbonyl-piperidin-4-yl)acetate (from Piperidine 35, Step A) in 2 mL of THF was added and the resulting solution was stirred cold for 30 min. Acetaldehyde (0.17 mL, 3.0 mmol) was added and the resulting mixture was warmed to 0° C. The reaction was quenched with 10 mL of sat'd NH4Cl and the resulting mixture was partitioned between 50 mL of ether and 25 mL of water. The organic layer was separated, dried over MgSO4 and concentrated. Flash chromatography on 20 g of silica gel using 2:1 v/v hexanes/EtOAc as the eluant afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125887B2
Source datasetuspto-grants-2006_10
ORD IDord-1a31d65c94444ed7989e5e310f346948
Source noteuspto-grants-2006_10