HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493507Generated: November 1, 2026
Hydrochloric Acid → HCID 11328213, compound
https://huagongshe.com/reaction/493507
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 131727450 | HCID 131727450 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11328213 | HCID 11328213 | 65% |
Reaction Steps
1 N NaOH (721 μL, 0.721 mmol) was added under nitrogen to a solution of methyl[(4′-{[(2-butyl-1-benzofuran-3-yl)carbonyl]amino}[1,1′-biphenyl]-4-yl)oxy]acetate (300 mg, 0.656 mmol), prepared in the previous step, in 30 mL of THF plus 10 mL of water at room temperature. After the addition the reaction was stirred at room temperature for 18 h (overnight). The reaction was acidified by the addition of 5 mL of 1 N HCl and then concentrated under reduced pressure. The solid that formed was collected by filtration and dried under reduced pressure to give the title compound (188 mg, 65%) as a white solid, mp 225-227° C.; MS (APCI) m/z 444 [M+H]+. Elemental Analysis for C27H25NO5.0.07 H2O: Calc'd: C, 72.92; H, 5.70; N, 3.15; Found: C, 72.45; H, 5.64; N, 3.06
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534894B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-6a180b2fec9a455ab158dcd411597f90 |
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| Source note | uspto-grants-2009_05 |
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