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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466010Generated: October 31, 2026

Methanol → 2-(Benzo[c][1,2,5]oxadiazol-5-yl)acetaldehyde

https://huagongshe.com/reaction/1466010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl morpholine oxideHCID 82029—
ReactantSodium periodateHCID 23667635—
Reactant5-Allyl-2,1,3-benzoxadiazoleHCID 59568714—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(Benzo[c][1,2,5]oxadiazol-5-yl)acetaldehydeHCID 77231158—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 5-Allyl-2,1,3-benzoxadiazole (4.1 g, 26 mmol) in a solution of MeOH (30 mL), THF (50 mL), and water (20 mL) was added Osium Tetraoxide (6.0 mL 4% aq. solution, 0.77 mmol) and NMO (4.5 g, 38 mmol). The mixture was allowed to stir at 25° C. for 16 hours. TLC showed complete reaction. The reaction was diluted with water (200 mL) and extracted with EtOAc (200 mL×2). The extractions were combined, washed with brine, dried over sodium sulfate, and concentrated. The resulting product was redissolved in water and methanol (50 mL each), and cooled to 0° C. To that solution was added an aqueous solution of sodium periodate (7.2 g, 33 mmol). TLC showed complete reaction within 15 minutes. The reaction was diluted with water (100 mL) and extracted with EtOAc (100 mL×2). The extractions were combined, washed with brine, dried over sodium sulfate, and concentrated to obtain the product which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999990B2
Source datasetuspto-grants-2015_04
ORD IDord-e1d2bed06a8441af83f709079c9d5970
Source noteuspto-grants-2015_04