HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673539Generated: October 29, 2026
Hydrochloric Acid → Tert-butyl 2-(biphenyl-3-carboxamido)-4-phenoxybenzoate
https://huagongshe.com/reaction/1673539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (1,1'-Biphenyl)-3-carboxylic acid | HCID 12854 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Tert-butyl 2-amino-4-phenoxybenzoate | HCID 58508592 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 2-(biphenyl-3-carboxamido)-4-phenoxybenzoate | HCID 67344270 | 6.6% |
Reaction Steps
4.0 mL of methylene chloride, 0.015 mL of N-dimethylformamide and 0.050 mL of oxalyl chloride were added to 99 mg of 3-biphenylcarboxylic acid at room temperature sequentially and stirred at the same temperature for 20 minutes. 0.16 mL of triethylamine and 0.13 g of tert-butyl 2-amino-4-phenoxybenzoate were added to the reaction mixture at room temperature sequentially and stirred at the same temperature for 10 minutes. Ethyl acetate and 1.0 mol/L hydrochloric acid were added to the reaction mixture. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium chloride aqueous solution, and the solvent was evaporated under reduced pressure. The obtained residue was purified with silica gel column chromatography [PSQ100B (spherical) manufactured by Fuji Silysia Chemical Ltd., eluent; chloroform] to obtain 14 mg of tert-butyl 2-(biphenyl-3-carboxamido)-4-phenoxybenzoate as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07999132B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-806b55725c3c45abbd4b065f9640584e |
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| Source note | uspto-grants-2011_08 |
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