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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872268Generated: October 31, 2026

Trifluoroacetic acid → HCID 18689623, compound

https://huagongshe.com/reaction/1872268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 54573955HCID 54573955—
SolventDichloromethaneHCID 6344—
ProductHCID 18689623HCID 18689623—

Reaction Conditions

Temperature12.5 °C

Reaction Steps

A solution of 3-(hydroxy-phenyl-methyl)-1-(4-methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2-carboxylic acid benzhydryloxy-amide (5 mg, 0.008 mmoL) in dichloromethane (1 mL) was cooled to 0° C. This solution was treated with trifluoroacetic acid (0.1 mL) followed by a 0.31 M solution of triethylsilane in dichloromethane (0.026 mL). The reaction mixture was warmed from 0 to 25° C. over 35 minutes and then the solvents were removed in vacuo and the residue was coevaporated with toluene. The residue was purified by flash chromatography (silica, 5 to 10% methanol in dichloromethane) to give 3-(hydroxy-phenyl-methyl)-1(4-methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2-carboxylic acid hydroxyamide as a white solid; MS: (M-H)- 430.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107291
Source datasetuspto-grants-2000_08
ORD IDord-514aecdcffaf478288c0c2424632ace0
Source noteuspto-grants-2000_08