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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612380Generated: October 30, 2026

Hydrochloric Acid → HCID 23221636, compound

https://huagongshe.com/reaction/612380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantHCID 23221647HCID 23221647—
ReactantHCID 131721512HCID 131721512—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23221636HCID 23221636—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(2,4-Dichlorophenoxy)4-methylsulphonylaminobenzene-sulphonic acid chloride N-methylamide (HN-56203) 3-(2,4-dichlorophenoxy)-4-methylsulphonylaminobenzenesulphonic acid chloride (0.56 g, 1.3 mmol) was dissolved in dioxan (15 ml) and at 0° C. it was added dropwise to a solution of methylamine hydrochloride (1.18 g, 17 mmol) in 1N aqueous NaOH (15 ml, 15 mmol) and dioxan (20 ml). The mixture was stirred for 1 hour at 0° C., acidified with 1N HCl and extracted with ethyl acetate. The combined organic phases were dried over MgSO4 and the solvent was evaporated off. The residue was purified by chromatography (silica gel, CH2Cl2 /ethyl acetate 9/1). Yield: 0.25 g=45% 13C (100 MHz, CDCl3) δ 148.35, 146.21, 134.97, 132.03, 131.28, 131.16, 128.98, 127.15, 123.15, 123.12, 119.56, 113.81, 40.45, 29.18

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06004948
Source datasetuspto-grants-1999_12
ORD IDord-af723933bade47a8a9662934b96094fe
Source noteuspto-grants-1999_12