HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657236Generated: November 1, 2026
Hydrogen Sulfide → Methyl p-[2-(p-amidinobenzamido)ethyl]phenoxyacetate
https://huagongshe.com/reaction/1657236
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Methyl 4-[2-(p-cyanobenzamido)ethyl]phenoxyacetate | HCID 10315069 | — |
| Reactant | Pyridine triethylamine | HCID 22561186 | — |
| Product | Methyl p-[2-(p-amidinobenzamido)ethyl]phenoxyacetate | HCID 10360837 | — |
Reaction Steps
H2S was passed for 45 minutes through a suspension of 2.0 g of methyl 4-[2-(p-cyanobenzamido)ethyl]phenoxyacetate in 24 ml of pyridine/triethylamine (7:1) at 0° C. The solution resulting after 12 hours was concentrated, and a suspension was made of the residue in methanol and filtered. The residue on the filter was immediately suspended in 30 ml of acetone, and 4 ml of methyl iodide were added. After 2.5 hours the precipitate was filtered off, washed with a little is acetone and, after drying, dissolved in 20 ml of methanol. 2.0 g of ammonium acetate were added and the mixture was then left to react at room temperature for 2 hours, during which a colorless precipitate formed, and this was filtered off and reprecipitated from methanol. Methyl p-[2-(p-amidinobenzamido)ethyl]phenoxyacetate was obtained as the acetate salt, melting point above 200° C., after drying under high vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05256812 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-5dea3f0ee6eb4dac9695d776cd23bf95 |
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| Source note | uspto-grants-1993_10 |
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