Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351914Generated: October 27, 2026

Azobisisobutyronitrile → HCID 58654521, compound

https://huagongshe.com/reaction/1351914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantHCID 15822375HCID 15822375—
ReactantDiphenyl[3-(phenylphosphanyl)propyl]phosphaneHCID 16693666—
ProductHCID 58654521HCID 58654521—

Reaction Conditions

Temperature210 °C

Reaction Steps

Ph2P(CH2)3P(H)Ph (3.68 g, 10.9 mmol), allyldiethylphosphine (1.71 g, 13.1 mmol) and AIBN (0.011 g) were mixed in a Schlenk flask and radiated with a 365 nm UV lamp for 20 hours. After confirming that the reaction was complete by 31P NMR analysis, it was distilled under vacuum (<0.5 mm Hg) at a final heating mantle temperature of 210° C. for an hour to remove impurities. The ligand remained in the pot. Yield: 3.36 g (66%). 31P NMR (122 MHz, CDCl3, δ, ppm): −16.74 (s), −23.09 (s) and −25.98 (s). There are peaks near the three major peaks, which have not been determined if are part of the ligand or due to impurities. 1H NMR (500 MHz, CDCl3, δ, ppm): 1.001 (d of q, JH-P&H=7.0 Hz 4H's methylenes of ethyl groups), 1.3 to 2.2 (m, H's on methyls and propylenes) (d of t, JH-P&H=211 & 6.6 Hz, H on the P), and 7.30 to 7.47 (m, 15H's on phenyl rings).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217848B2
Source datasetuspto-grants-2007_05
ORD IDord-adcf19395f5a487c95a6370d14ba449e
Source noteuspto-grants-2007_05