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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438205Generated: November 1, 2026

Acetyl bromide → HCID 86223898, compound

https://huagongshe.com/reaction/1438205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl bromideHCID 10482—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86223897HCID 86223897—
SolventAcetic AcidHCID 176—
ProductHCID 86223898HCID 8622389872%

Reaction Conditions

Temperature90 °C

Reaction Steps

Acetyl bromide (14 mL) was added to a solution of 4-nitro-2,6-bis-(2,2,2-trifluoro-ethyl)-pyridine 1-oxide (2.7 g, 8.9 mmol) dissolved in AcOH (25 mL). The reaction mixture was heated to 90° C. for 5 hours. The reaction was cooled to room temperature, poured into ice, made basic with NaOH pellets and extracted with EtOAc. The organic layers were washed with brine, dried over Na2SO4 and concentrated to a red oil. Purification by flash column chromatography (0% to 30% EtOAc in hexanes) gave the product as a yellow oil (2.18 g, 72%). 1H NMR (400 MHz, CDCl3): δ 3.92 (t, J=10.1 Hz, 4H), 7.59 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622605B2
Source datasetuspto-grants-2009_11
ORD IDord-f40837bdf0ad420c8e3c82a386839ee2
Source noteuspto-grants-2009_11