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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
Reactant(1,1'-Biphenyl)-4-sulphonyl chlorideHCID 74192—
ReactantN-Boc-allylglycine methyl esterHCID 22243128—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-[[(1,1'-biphenyl)-4-yl]sulfonyl]amino-4-pentenoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566381B1
Source datasetuspto-grants-2003_05
ORD IDord-b0f99f7f01f242c099f9b102c92941f9
Source noteuspto-grants-2003_05