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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824791Generated: November 2, 2026

Benzaldehyde → HCID 22144525, compound

https://huagongshe.com/reaction/1824791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantWaterHCID 962—
Reactant2-Bromo-4-methoxy-6-nitrophenolHCID 11265140—
ReactantHCID 101645068HCID 101645068—
CatalystManganeseHCID 23930—
Catalystchromium(II) dichlorideHCID 10197677—
SolventDimethylformamideHCID 6228—
ProductHCID 22144525HCID 22144525—

Reaction Steps

tert-Butyl-chloro-silane (0.25 ml) was added to a mixture of 2-bromo-4-methoxy-6-nitro-phenol (0.124 g), chromium (II) chloride (0.012 g) and manganese (0) powder (0.137 g) in dimethylformamide (3 mL). The mixture was subjected to microwaves for 4 min at 150° C. Benzaldehyde (0.06 mL) was added and the reaction was subjected to microwaves for 6 min at 150° C. Water (0.5 mL) was added, then after 30 min the mixture was filtered through a pad of celite. The above procedure was repeated three more times. The combined filtrate was partitioned between dilute aq. HCl (100 mL) and ethyl acetate (100 mL). The organic layer was dried over sodium sulfate, filtered through celite and concentrated. Chromatography on silica gel (eluant: gradient 0 to 30% ethyl acetate:hexane) afforded 7-bromo-5-methoxy-2-phenyl-benzooxazole (0.13 g). MS: 304 (95%), 306.4 (100%) (MH+); HPLC tR: 2.79 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045539B2
Source datasetuspto-grants-2006_05
ORD IDord-e61e9eb7c38d49e893c5dae203141b77
Source noteuspto-grants-2006_05