Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836411Generated: November 1, 2026

Butyl isocyanate → HCID 23499245, compound

https://huagongshe.com/reaction/1836411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl isocyanateHCID 8110—
Reactant4-[3-Aminobenzoyl]-1-methylpiperidineHCID 10130651—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23499245HCID 23499245121.6%

Reaction Steps

4-[3-aminobenzoyl]-1-methylpiperidine (25 mg, 0.115 mmol) and poly(4-vinyl pyridine) (50 mg, 0.400 mmol, 2% cross-linked) in tetrahydrofuran (2 mL) were allowed to stand 10 min. Butyl isocyanate (39 μL, 0.344 mmol) was added and the reaction mixture was mixed for 96 h at ambient temperature. An addition amount of butyl isocyanate(100 μL, 0.888 mmol) was added to the reaction mixture and mixing was continued for another 6 days. The reaction mixture was filtered and the filter cake was rinsed with methanol. Glacial acetic acid (0.5 mL) was added to the filtrate solution and the solution was mixed. This mixture was poured over a Varian Mega Bond Elut™ strong cation exchange column. The column was rinsed extensively with methanol to remove impurities, then treated with a 2M ammonia in methanol to elute the product from the column. The solvent was evaporated to give 44.4 mg (>100%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777428B1
Source datasetuspto-grants-2004_08
ORD IDord-7682a9c62f704d2bacc9c75a6b1ab925
Source noteuspto-grants-2004_08