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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578362Generated: November 3, 2026

2-Amino-5-nitrobenzene-1,3-dicarbonitrile → HCID 21559844, compound

https://huagongshe.com/reaction/1578362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-nitrobenzene-1,3-dicarbonitrileHCID 13691769—
ReactantHCID 21559842HCID 21559842—
ReactantHCID 21559846HCID 21559846—
ReactantSodium hydroxide methanolHCID 23721981—
ProductHCID 21559844HCID 21559844—

Reaction Steps

2,6-Dicyano-4-nitro-phenol, used in Example 12, was prepared according to generally known processes: 2,6-dicyano-4-nitro-aniline is converted by a Sandmeyer reaction into 2,6-dicyano-4-nitro-chlorobenzene of melting point 218°-219.5°C, reacted with methanol/sodium hydroxide to give 2,6-dicyano-4-nitro-anisole of melting point 144°-148°C, and the latter subsequently split with sodium iodide in dimethylformamide to give 2,6-dicyano-4-nitro-phenol of melting point 228°-231°C. The last two stages correspond to a process indicated in Belgian Pat. No. 764,117.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03936447
Source datasetuspto-grants-1976_02
ORD IDord-ae6d87d2c3f04b989dbbce6b76475ce2
Source noteuspto-grants-1976_02