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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605309Generated: October 30, 2026

Benzaldehyde → 5-Chloro-6-nitro-2-phenyl-1,3-benzoxazole

https://huagongshe.com/reaction/605309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantMethaneHCID 297—
Reactant2-Amino-4-chloro-5-nitrophenolHCID 3894848—
Product5-Chloro-6-nitro-2-phenyl-1,3-benzoxazoleHCID 13609246—

Reaction Steps

To a flask equipped with a vigreux column was added 2-amino-4-chloro-5-nitro-phenol, benzaldehyde, Darco KB and xylenes. The mixture was then refluxed overnight and the mixture was cooled, filtered and the solvent removed under vacuum. The resultant solid was recrystallized from Et2O to yield 5-chloro-6-nitro-2-phenyl-benzooxazole which was subjected to the procedure from Example 349B substituting 5-chloro-6-nitro-2-phenyl-benzooxazole for the product from Example 349A to provide the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910595B2
Source datasetuspto-grants-2011_03
ORD IDord-4eeaa7693a61453aa658627e4146e84c
Source noteuspto-grants-2011_03