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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395273Generated: November 2, 2026

Trifluoroacetic acid → 7-Methanesulfonyloxy-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/395273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-(tert-Butyloxycarbonyl)-7-methanesulfonyloxy-2,3,4,5tetrahydro-1H-3-benzazepineHCID 11279289—
SolventDichloromethaneHCID 6344—
Product7-Methanesulfonyloxy-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 1129947281%

Reaction Steps

A solution of 3-(tert-butyloxycarbonyl)-7-methanesulphonyloxy-2,3,4,5-tetrahydro-1H-3-benzazepine (3.8 g, 0.011 mol), trifluoroacetic acid (3.76 g, 0.033 mol) and dichloromethane (50 ml) was heated at 50° C. for 5 h. The solvents were then evaporated in vacuo and the residue partitioned between water (200 ml) and ethyl acetate (150 ml). The aqueous layer was removed and washed with ethyl acetate (100 ml) and then basified to pH 14 with 40% sodium hydroxide. The suspension was then extracted with ethyl acetate (3×150 ml) and the combined organic layers dried (Na2SO4). The solvents were evaporated in vacuo to give the title compound (2.15 g, 80%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605607B1
Source datasetuspto-grants-2003_08
ORD IDord-6d919e89670b45d884d40bc653debc9f
Source noteuspto-grants-2003_08