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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267481Generated: October 28, 2026

Piperidine → HCID 21554782, compound

https://huagongshe.com/reaction/267481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 14786861HCID 14786861—
ReactantHCID 21514640HCID 21514640—
CatalystPlatinum oxide (PtO)HCID 82844—
ProductHCID 21554782HCID 21554782—

Reaction Steps

Following the procedure of Example 4, a mixture of 201 parts (1 mole) of N-(1,1-dimethyl-3-oxobutyl)-3-methoxypropionamide, 170 parts (2 moles) of piperidine, 0.5 part of platinum oxide and 1 part of dimethylammonium perchlorate is hydrogenated in the Parr apparatus, starting at a pressure of 70 psi. and recharging when the pressure has reached 39 psi. After workup as described in Example 4, the desired product, N-(1,1-dimethyl-3-piperidinobutyl)-3-methoxypropionamide, is obtained boiling at 112°-115° C./0.25 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03943114
Source datasetuspto-grants-1976_03
ORD IDord-0644c9151e104d18a16a02fb865ab1ac
Source noteuspto-grants-1976_03