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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Furanmethanaminium, N,N,N-trimethyl-, iodide (1:1) | HCID 10937 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21520079 | HCID 21520079 | — |
| Solvent | Diethylene glycol diethyl ether | HCID 8179 | — |
| Product | HCID 21520115 | HCID 21520115 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03972886 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-feedc16270024ab79d3caeb56f5b3a20 |
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| Source note | uspto-grants-1976_08 |
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