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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536441Generated: October 30, 2026

Triethylamine → (NE)-N-[(7-bromo-2-methyl-1,3-benzoxazol-4-yl)methylidene]hydroxylamine

https://huagongshe.com/reaction/536441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant7-Bromo-2-methyl-benzo[d]oxazole-4-carbaldehydeHCID 58497957—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product(NE)-N-[(7-bromo-2-methyl-1,3-benzoxazol-4-yl)methylidene]hydroxylamineHCID 58498024105.2%

Reaction Steps

To a suspension of 7-bromo-2-methyl-benzo[d]oxazole-4-carbaldehyde (3.23 g) in a mixture of methanol and water (7:3) (60 ml) were added successively hydroxylamine hydrochloride (1.03 g) and triethylamine (2.06 ml) and the reaction mixture was stirred at ambient temperature for 1 hour. The reaction mixture was diluted with ethyl acetate (200 ml) and water (200 ml). The phases were separated and the aqueous phase was extracted with ethyl acetate (150 ml). The combined organic extracts were washed with brine (200 ml), dried over sodium sulfate and concentrated to give (E)-7-bromo-2-methyl-benzo[d]oxazole-4-carbaldehyde oxime (3.61 g) as a brown solid. 1H-NMR (400 MHz, CDCl3): 9.47 (s, 1H) 7.47 (d, 1H), 7.33 (d, 1H), 2.74 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859592B2
Source datasetuspto-grants-2014_10
ORD IDord-eee9d53e6beb4fa4895dfaf0d2eeeee4
Source noteuspto-grants-2014_10