HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236752Generated: October 28, 2026
Sodium borohydride → HCID 23338998, compound
https://huagongshe.com/reaction/236752
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23339073 | HCID 23339073 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23338998 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04157393 |
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| Source dataset | uspto-grants-1979_06 |
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| ORD ID | ord-605ce604b05d4eeab810b096b19fa2a4 |
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| Source note | uspto-grants-1979_06 |
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