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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340151Generated: October 26, 2026

Hydrochloric Acid → (6-Bromobenzo[d]isothiazol-3-yl)(4-chlorophenyl)methanone

https://huagongshe.com/reaction/340151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant6-bromo-N-methoxy-N-methylbenzo[d]isothiazole-3-carboxamideHCID 86658353—
ReactantHCID 178478191HCID 178478191—
SolventTetrahydrofuranHCID 8028—
Product(6-Bromobenzo[d]isothiazol-3-yl)(4-chlorophenyl)methanoneHCID 6743673281%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Chlorophenyl magnesium bromide (1.0N in THF, 16 mL, 16 mmol) was added to a stirred solution of 6-bromo-N-methoxy-N-methylbenzo[d]isothiazole-3-carboxamide (3.5 g, 12 mmol) in THF (100 mL). The reaction mixture was stirred at 0° C. for 1 hour. The reaction was poured into 1N HCl and extracted into ether. The combined organic layers were washed with brine, dried and concentrated. The crude product was suspended in ether and stirred for 15 minutes. The solid was collected by filtration to give (6-bromobenzo[d]isothiazol-3-yl)(4-chlorophenyl)methanone (3.3 g, 81%). 1H NMR (CDCl3, 400 MHz) δ □8.60 (d, J=8.8 Hz, 1H), 8.23 (d, J=8.4 Hz, 2H), 8.19 (s, 1H), 7.68 (d, J=8.8 Hz, 1H), 7.51 (d, J=8.4 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895566B2
Source datasetuspto-grants-2014_11
ORD IDord-d6432ed1591b47ea825967e17ad2e068
Source noteuspto-grants-2014_11