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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594243Generated: October 31, 2026

(2-Methylbenzo[D]thiazol-6-YL)methanol → 2-Methyl-1,3-benzothiazole-6-carbaldehyde

https://huagongshe.com/reaction/594243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Methylbenzo[D]thiazol-6-YL)methanolHCID 676590—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-1,3-benzothiazole-6-carbaldehydeHCID 4285597—

Reaction Steps

A solution of (2-methylbenzo[d]thiazol-6-yl)methanol (300 mg; 1.67 mmol) in anh. THF (15 ml) was treated with MnO2 (2.269 g; 26.11 mmol), and the resulting mixture was stirred at rt, under nitrogen, for 6.5 h. The resulting reaction mixture was then filtered over celite, and the separated solids were washed with THF. The filtrate was concentrated to dryness under reduced pressure giving 2-methylbenzo[d]thiazole-6-carbaldehyde as a yellow solid. LC-MS (conditions A): tR=0.56 min.; [M+H]+: 178.15 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-66d7553f77c5455185d93199045b1543
Source noteuspto-grants-2016_01