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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576046Generated: October 31, 2026

Chlorosulfonic acid → HCID 86707265, compound

https://huagongshe.com/reaction/576046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant1-(7-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)-2,2,2-trifluoroethanoneHCID 10968831—
SolventChloroformHCID 6212—
ProductHCID 86707265HCID 86707265—

Reaction Conditions

Temperature60 °C

Reaction Steps

Chlorosulfonic acid (35.6 mL) was added dropwise to a solution of 1-(7-bromo-3,4-dihydroisoquinolin-2(1 H)-yl)-2,2,2-trifluoroethanone obtained (25.4 g, 82.3 mmol) in chloroform (35 mL) while cooling in ice, and the mixture was stirred at room temperature for 1 hr and at 60° C. for 4 hr. After cooling, the reaction mixture was added dropwise to ice water and the mixture was extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate and then the desiccant was filtered off, followed by concentration under reduced pressure. The concentrate was powdered with hexane and ethyl acetate (5:1) and then collected by filtration to afford 7-bromo-2-(trifluoroacetyl)-1,2,3,4-tetrahydroisoquinoline-6-sulfonyl chloride as a pale yellow powder (22.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035059B2
Source datasetuspto-grants-2015_05
ORD IDord-0965c2cd1fc04af3bb6363021b594504
Source noteuspto-grants-2015_05