Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438763Generated: November 3, 2026

P-Anisidine → HCID 68126044, compound

https://huagongshe.com/reaction/1438763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
Reactantm-ToluidineHCID 7934—
ReactantHCID 21400469HCID 21400469—
ProductHCID 68126044HCID 68126044—

Reaction Steps

If the procedure indicated above is followed but the 8-nitro compound is replaced by a mixtue of 1-isopropylamino-4-bromo-5- and -8-nitroanthraquinone and 180 g of p-anisidine are used instead of m-toluidine as the base, 48 g of a mixture consisting of 1-isopropylamino-4-p-anisidino-5-nitroanthraquinone and 1-isopropylamino-4-p-anisidine-8 -nitroanthraquinone are obtained after dilution with 300 ml of methanol and filtration at 10°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04056544
Source datasetuspto-grants-1977_11
ORD IDord-f8ff3336ab75439aa82a034ddf385e2e
Source noteuspto-grants-1977_11