HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253917Generated: October 26, 2026
4-Benzeneazodiphenylamine → HCID 86747081, compound
https://huagongshe.com/reaction/2253917
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Benzeneazodiphenylamine | HCID 7575 | — |
| Reactant | 2-(2,2-Dimethyl-1,3-dioxolan-4-yl)ethan-1-ol | HCID 4219754 | — |
| Reactant | N-methyl-N-(2-bromoethyl)phosphoramidic dichloride | HCID 10332578 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86747081 | HCID 86747081 | — |
Reaction Steps
Butyllithium (10.8 ml, 21.60 mmol, 2.0M) was added dropwise at 0° C. to a stirred solution of 4-(2-hydroxyethyl)-2,2-dimethyl-1,3-dioxolane (2.87 g, 19.60 mmol) and a crystal of 4-phenylazodiphenylamine indicator in THF (7 ml) under N2. The resulting solution was added dropwise at -78° C. to a stirred solution of N-methyl-N-(2-bromoethyl) phosphoramidic dichloride (5.00 g, 19.60 mmol) in THF (10 ml) under N2. The mixture was allowed to stir under N2 at -78° C. for 3 hr, at which time the purple mixture turned yellow. The mixture was warmed to room temperature and the solvent removed under reduced pressure. The residue was purified by chromatography (1:4 EtOAc: hexanes) and the product 16a isolated as an oil (4.77 g, 67%): Rf 0.61 (1:1 EtOAc:hexanes); 1H NMR (CDCl3) 4.26(dt, 2H, J= 8.44 Hz), 4.17(t, 1H, J=6.53 Hz), 4.06(t, 1H, J=7.06 Hz), 3.54(t, 1H, J=7.10 Hz), 3.44(m, 4H), 2.76(d, 3H, J=12.76 Hz), 1.95(dt, 2H, J=6.24 Hz), 1.67(d, 6H, 15.63 Hz); 31P NMR (CDCl3) -8.07 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05233031 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-1584e8fa79314ef18ad20f7743f9285b |
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| Source note | uspto-grants-1993_08 |
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