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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28140Generated: October 29, 2026

Sodium borohydride → HCID 23338998, compound

https://huagongshe.com/reaction/28140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23339073HCID 23339073—
SolventMethanolHCID 887—
ProductHCID 23338998HCID 23338998—

Reaction Steps

To a stirred and warmed (30°-40° C.) solution of 72 parts of N-[1-(1-methylethyl)-4-piperidinylidene]-benzenamine in 480 parts of methanol are added potionwise 20 parts of sodium borohydride. Upon completion, stirring is continued overnight at at room temperature. The reaction mixture is evaporated and the residue is dissolved in water. The solution is extracted with 4-methyl-2-pentanone. The extract is washed with water and acidified with a diluted hydrochloric acid solution. The aqueous acid phase is alkalized with a diluted sodium hydroxide solution till pH 9 and the product is extracted with 4-methyl-2-pentanone. The extract is washed with water, dried, filtered and evapoarated. The residue is distilled (bp. 135-140° C. at 0.2 mm. pressure) and the distillate is crystallized from petroleumether, yielding 21 parts of 1-(1-methylethyl)-N-phenyl-4-piperidinamine; mp. 69.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04225606
Source datasetuspto-grants-1980_09
ORD IDord-1ff25e688fc64cdaac4a8e2210b467cd
Source noteuspto-grants-1980_09