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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Reactant | 7-Acetyl-4-(benzyloxy)-1,3-benzothiazol-2(3H)-one | HCID 69321983 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Benzyloxy)-7-(bromoacetyl)-1,3-benzothiazol-2(3H)-one | HCID 85939637 | 93.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402598B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-400103016d584ac1b294435029fd05bf |
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| Source note | uspto-grants-2008_07 |
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