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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086440Generated: October 31, 2026

1-Phenylpiperidine → HCID 22727358, compound

https://huagongshe.com/reaction/2086440

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperidineHCID 20038—
Reactant1-BenzylpiperazineHCID 75994—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 22727329HCID 22727329—
SolventDichloromethaneHCID 6344—
ProductHCID 22727358HCID 2272735894.7%

Reaction Steps

About 2 min after dissolving 3-(3-(2-thienyl)isoxazol-5-yl)butanal (23.5 mg, 0.106 mmol) and 1-phenylpiperidine (16.2, 0.106 mmol) in 2 mL of dry methylene chloride, were added NaBH(OAc)3 (67.4 mg, 0.318 mmol), cold acetic acid (7.3, 0.127 1mmol) and molecular sieves (5 beads). The reaction mixture was reacted for 3 hr and followed the same processes as in Example 1 to obtain 36.9 mg (94.7%) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06723724B2
Source datasetuspto-grants-2004_04
ORD IDord-77ec5df1d8a744ae95a834b3402de957
Source noteuspto-grants-2004_04