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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236752Generated: October 28, 2026

Sodium borohydride → HCID 23338998, compound

https://huagongshe.com/reaction/236752

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 portionwise 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 evaporated. 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 numberUS04157393
Source datasetuspto-grants-1979_06
ORD IDord-605ce604b05d4eeab810b096b19fa2a4
Source noteuspto-grants-1979_06