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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282792Generated: November 1, 2026

2-Furanmethanaminium, N,N,N-trimethyl-, iodide (1:1) → HCID 21520115, compound

https://huagongshe.com/reaction/1282792

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furanmethanaminium, N,N,N-trimethyl-, iodide (1:1)HCID 10937—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21520079HCID 21520079—
SolventDiethylene glycol diethyl etherHCID 8179—
ProductHCID 21520115HCID 21520115—

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 3-mercapto-4-phenoxy-5-sulfamylbenzoic acid (1.6 g) in diethylene glycol diethyl ether (15 ml), anhydrous potassium carbonate (0.5 g) and trimethylfurfurylammonium iodide (2 g) were added. The resulting mixture is stirred at 110°C. for 4 hours, cooled and poured into 0.3 N sodium hydroxide (75 ml). After extraction twice with diethyl ether, the aqueous layer is adjusted to pH 3 by addition of acetic acid. The reaction product is extracted with ethyl acetate, and the resulting organic solution is evaporated in vacuo. The residue is triturated with aqueous acetone giving rise to crystallisation. The 3-(2-furylmethylthio)-4-phenoxy-5-sulfamylbenzoic acid thus obtained is recrystallized from aqueous ethanol and dried. The compound is obtained with a melting point of 214°-216°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03972886
Source datasetuspto-grants-1976_08
ORD IDord-feedc16270024ab79d3caeb56f5b3a20
Source noteuspto-grants-1976_08