HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65175Generated: October 29, 2026
4-Amino-4'-hydroxybiphenyl → 2-Chloro-4-nitro-4'-(4-hydroxyphenyl)azobenzene
https://huagongshe.com/reaction/65175
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Amino-4'-hydroxybiphenyl | HCID 14565 | — |
| Reactant | 2-Chloro-4-nitro-1-nitrosobenzene | HCID 20233380 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Chloro-4-nitro-4'-(4-hydroxyphenyl)azobenzene | HCID 136003052 | 81.6% |
Reaction Steps
A suspension of 0.840 g of 2-chloro-4-nitro-1-nitrosobenzene in 20 ml of glacial acetic acid was heated to 70° C. and treated while stirring with a solution, heated to 110° C., of 0.926 g of 4-amino-4'-hydroxybiphenyl [prepared according to Chem. Berichte 27 (1894) 2627] in 43 ml of glacial acetic acid. The dark solution was stirred at 70° C. for a further 2.25 hours, then cooled to room temperature and extracted with methylene chloride. The extracts were washed with water, 10% sodium hydrogen carbonate solution and again with water, dried over sodium sulphate and concentrated in vacuo. Thus yielding 1.3 g of crude 2-chloro-4-nitro-4'-(4-hydroxyphenyl)azobenzene as brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04613208 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-eee20e3f3d714805a25e7ed6eb4a5784 |
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| Source note | uspto-grants-1986_09 |
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