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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128407Generated: October 30, 2026

Sodium Hydroxide → p-Aminobenzamidine

https://huagongshe.com/reaction/128407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantBenzenecarboximidamide, 4-amino-, hydrochloride (1:1)HCID 122765—
SolventWaterHCID 962—
Productp-AminobenzamidineHCID 1725—

Reaction Steps

Addition of 50% sodium hydroxide (4.0 g., 0.05 mole) to a solution of 4-aminobenzamidine hydrochloride (0.5 mole) in 10 ml. of water affords 4-aminobenzamidine free base. Acetone (50 ml.) is added to the liberated free base and the mixture cooled to 5° C. 4-Nitrostyrylsulfonyl chloride is added to the mixture in a period of 5 min. while maintaining a temperature below 15° C. The mixture is stirred for 10 min., the reaction mixture concentrated under reduced pressure provides a residue which diluted with 100 ml. of water and neutralized with 3 N hydrochloric acid affords a pale yellow solid precipitate. The precipitate is collected, washed thoroughly with water and then triturated first with isopropanol and then with ether to yield 7.3 g. (84%) of N-(4-NITROSTYRYLSULFONYL)-4-AMINOBENZAMIDINE, m.p. 188°-189° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259482
Source datasetuspto-grants-1981_03
ORD IDord-08cac3570d854f73b556696eea77141f
Source noteuspto-grants-1981_03