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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704403Generated: October 26, 2026

Methanol → Ethyl 4-[(2,6-dichlorophenyl)amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1704403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 4-[(2,6-dichlorophenyl)imino]-1-piperidinecarboxylateHCID 23339072—
SolventIsopropanolHCID 3776—
ProductEthyl 4-[(2,6-dichlorophenyl)amino]-1-piperidinecarboxylateHCID 23338997—

Reaction Steps

To a stirred and refluxing mixture of 250 parts of ethyl 4-[(2,6-dichlorophenyl)imino]-1-piperidinecarboxylate in 160 parts of methanol and 160 parts of 2-propanol are added portionwise 30 parts of sodium borohydride. Upon completion, stirring at reflux temperature is continued for one hour. The warm reaction mixture is poured onto water and the product is extracted with methylbenzene. The extract is dried and evaporated. The residue is crystallized from a mixture of 160 parts of 2,2'-oxybispropane and 160 parts of petroleumether, yielding 96 parts of ethyl 4-[(2,6-dichlorophenyl)-amino]-1-piperidinecarboxylate; mp. 107.2°-116.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04126689
Source datasetuspto-grants-1978_11
ORD IDord-a8e6786ffce34fc3b682e6f65f2c9f27
Source noteuspto-grants-1978_11