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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597210Generated: October 30, 2026

Propionic Acid → HCID 135853039, compound

https://huagongshe.com/reaction/597210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionic AcidHCID 1032—
ReactantSulfuric AcidHCID 1118—
Reactant2-Mesyl-4-nitroanilineHCID 66785—
ReactantHCID 21446735HCID 21446735—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventPyridineHCID 1049—
ProductHCID 135853039HCID 135853039—

Reaction Conditions

Temperature25 °C

Reaction Steps

The 2-t-butylsulfamoyl-5-(3-fluorosulfonylbenzenesulfonamido)-4-(2-methylsulfonyl-4-nitrophenylazo)-1-naphthol was prepared by diazo coupling. 7.6 G. (0.11 mol) of sodium nitrite was added to 66 ml. of sulfuric acid at 5° C. and warmed to 70° C. to effect solution. After cooling to 25° C., 23.8 g. (0.11 mol) of 2-methanesulfonyl-4-nitroaniline was added, and the mixture stirred for 2 hours. The diazonium salt mixture was poured into 250 ml. of 1:5 acid (1 part propionic acid to 5 parts acetic acid) at 5° C. A solution of the coupler was prepared by dissolving 51.6 g. (0.1 mol) of 2-t-butylsulfamoyl-5-(3-fluorosulfonylbenzenesulfonamido)-1-naphthol in 66 ml. of pyridine, cooling to 10° C., and adding 520 ml. of the 1:5 acid at 30° C. The diazonium mixture was added to the coupler solution and stirred for one hour at 7° C., the solid collected on a filter funnel and then slurried twice in 500 ml. of 1% hydrochloric acid. The slurry was filtered and the solid dried in a desiccator at 60° C. to yield 25.8 g. of dye. The filtrates from the reaction mixture were diluted to 8000 ml. with water to precipitate additional dye, which was collected on a filter funnel and dried in a desiccator to yield an additional 40 g. (88% total).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04013635
Source datasetuspto-grants-1977_03
ORD IDord-6bf07563258b41c6bfb36890fd4f33bc
Source noteuspto-grants-1977_03