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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749241Generated: October 30, 2026

Phenyltrimethylammonium bromide dibromide → 4-(Benzyloxy)-7-(bromoacetyl)-1,3-benzothiazol-2(3H)-one

https://huagongshe.com/reaction/749241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
Reactant7-Acetyl-4-(benzyloxy)-1,3-benzothiazol-2(3H)-oneHCID 69321983—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(Benzyloxy)-7-(bromoacetyl)-1,3-benzothiazol-2(3H)-oneHCID 8593963793.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 7-acetyl-4-(benzyloxy)-1,3-benzothiazol-2(3H)-one (68 mg) in dry THF (3 ml) under nitrogen, was added phenyltrimethylammonium tribromide (90 mg) and the mixture heated at 80° C. under nitrogen for 2 h. The mixture was diluted with water, extracted with ethyl acetate, dried (MgSO4), filtered and evaporated in vacuo. The residue was purified on a 5 g silica SPE cartridge, eluting with stepped gradient of 10% to 100% ethyl acetate-cyclohexane mixtures, to give the title compound (49 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402598B2
Source datasetuspto-grants-2008_07
ORD IDord-400103016d584ac1b294435029fd05bf
Source noteuspto-grants-2008_07