Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501080Generated: October 25, 2026

Acetic Acid → Benzyl 4-{[1-(methoxycarbonyl)but-3-en-1-yl]amino}piperidine-1-carboxylate

https://huagongshe.com/reaction/501080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 2-aminopent-4-enoateHCID 10877146—
Solvent1,1-DichloroethaneHCID 6365—
ProductBenzyl 4-{[1-(methoxycarbonyl)but-3-en-1-yl]amino}piperidine-1-carboxylateHCID 22293179103.4%

Reaction Steps

Sodium triacetoxyborohydride (11.2 g, 52.6 mmol) was added to a solution of methyl 2-aminopent-4-enoate (3.4 g, 26.3 mmol), acetic acid (2.37 g, 39.5 mmol) and benzyl 4-oxopiperidine-1-carboxylate (9.21 g, 39.5 mmol) in dichloroethane (60 mL) at room temperature. After 3 h, the reaction was quenched with saturated aqueous sodium bicarbonate, extracted with methylene chloride (3×), dried over sodium sulfate, filtered and evaporated to give the crude product. This was purified by chromatography (silica gel, 0 to 8% methanol in methylene chloride gradient elution), which gave the title compound (9.42 g). MS 347.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772224B2
Source datasetuspto-grants-2010_08
ORD IDord-2e62c9e148304d0fb402c9e67c8a22e5
Source noteuspto-grants-2010_08