HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584899Generated: October 30, 2026
Hydrochloric Acid → HCID 10157037, compound
https://huagongshe.com/reaction/584899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 10273326 | HCID 10273326 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10157037 | HCID 10157037 | 90% |
Reaction Steps
1.25 g (3 mmol) of ethyl 3-{3′-[(benzoyl-methylamino)methyl]biphenyl-4-yl}-2-methylpropionate, 3 ml of sodium hydroxide (10N), 32 ml of THF and 2 ml of methanol are introduced into a round-bottomed flask. The reaction medium is refluxed for 8 hours, poured into water, acidified to pH 4 with 1N hydrochloric acid and extracted with dichloromethane, and the organic phase is separated out after settling of the phases has taken place, dried over magnesium sulfate and evaporated. The residue obtained is purified by chromatography on a column of silica eluded with a mixture of heptane and ethyl acetate (60/40). 900 mg (90%) of 2-methyl-3-(3′-{[methyl-(1-phenylmethanoyl)-amino]methyl}biphenyl-4-yl)propionic acid, with a melting point of 60-61° C., are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06927228B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-8721ab39d20e476d92b66b795c87c062 |
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| Source note | uspto-grants-2005_08 |
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