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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521392Generated: October 26, 2026

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

https://huagongshe.com/reaction/521392

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 numberUS09328091B2
Source datasetuspto-grants-2016_05
ORD IDord-b7c331785f334371a5bac24e9813e6be
Source noteuspto-grants-2016_05