HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413365Generated: October 28, 2026
Trifluoroacetic acid → Methyl 2-[[(1,1'-biphenyl)-4-yl]sulfonyl]amino-4-pentenoate
https://huagongshe.com/reaction/413365
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (1,1'-Biphenyl)-4-sulphonyl chloride | HCID 74192 | — |
| Reactant | N-Boc-allylglycine methyl ester | HCID 22243128 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-[[(1,1'-biphenyl)-4-yl]sulfonyl]amino-4-pentenoate | HCID 23508264 | — |
Reaction Steps
To a solution of N-Boc-allylglycine methyl ester 1a (4.0 g, 17.6 mmol) in CH2Cl2 (15 mL is added trifluoroacetic acid (10 mL) slowly, and the resulting mixture is stirred overnight at room temperature. The reaction mixture is concentrated under reduced pressure to dryness then dissolved in dioxane (15 mL) and water (15 mL). To the solution is added triethyl amine (9.8 mL, 70.4 mmol), followed by biphenyl-4-sulfonyl chloride (5.9 g, 21.12 mmol) and the mixture is stirred overnight. The reaction mixture is diluted with water, extracted three times with EtOAc. The combined EtOAc layer is washed with 1 N HCl, H2O, brine, dried, and concentrated to an oil which solidified upon standing. The crude product is recrystallized from EtOAc/hexane to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06566381B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-b0f99f7f01f242c099f9b102c92941f9 |
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| Source note | uspto-grants-2003_05 |
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