HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351914Generated: October 27, 2026
Azobisisobutyronitrile → HCID 58654521, compound
https://huagongshe.com/reaction/1351914
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 15822375 | HCID 15822375 | — |
| Reactant | Diphenyl[3-(phenylphosphanyl)propyl]phosphane | HCID 16693666 | — |
| Product | HCID 58654521 | HCID 58654521 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217848B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-adcf19395f5a487c95a6370d14ba449e |
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| Source note | uspto-grants-2007_05 |
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