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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061896Generated: November 1, 2026

Acetonitrile → Caprolactam

https://huagongshe.com/reaction/2061896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantCaprolactamHCID 7768—
ReactantHCID 178528035HCID 178528035—
SolventTetrahydrofuranHCID 8028—
ProductCaprolactamHCID 7768—
Product2,5-DimethyltetrahydrofuranHCID 13855—

Reaction Steps

Prior to optimization of the initial H2/H2S atmosphere and the mol % catalyst of presulfided Pt (Pt—S/C) employed, a range of solvents is examined (Table 5). No formation of caprolactam is observed using acetonitrile (entry 1, Table 5) as solvent. The highest yield of caprolactam is achieved using THF (entry 2, Table 5). Use of 2,5-dimethyltetrahydrofuran (entry 3, Table 5) results in a tenfold reduction in the yield of caprolactam relative to use of THF as solvent (entry 3 vs. entry 2, Table 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283466B2
Source datasetuspto-grants-2012_10
ORD IDord-087dcbe524b9493688bef85ca497372e
Source noteuspto-grants-2012_10