Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671785Generated: October 31, 2026

(2-Bromo-4-fluorobenzo[d]thiazol-6-yl)methanol → 2-Bromo-4-fluorobenzo[d]thiazole-6-carbaldehyde

https://huagongshe.com/reaction/1671785

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Bromo-4-fluorobenzo[d]thiazol-6-yl)methanolHCID 57527173—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-4-fluorobenzo[d]thiazole-6-carbaldehydeHCID 5752722361%

Reaction Steps

A mixture of (2-bromo-4-fluorobenzo[d]thiazol-6-yl)methanol (0.269 g, 1.03 mmol) and manganese (IV) oxide (activated, 85%, 1.47 g, 14.4 mmol) in THF (15 mL) was stirred at rt for 16 hr. Solid material was removed by filtration through Celite® 545, and the filtrate was concentrated under vacuum. The residue was diluted with AcOEt, washed with brine, and dried over anhydrous MgSO4. Evaporation of solvent under vacuum gave the title compound (0.136 g, 61% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994337B2
Source datasetuspto-grants-2011_08
ORD IDord-862a1e110bbb4c739561a733cac3a0b1
Source noteuspto-grants-2011_08