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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834326Generated: November 3, 2026

Sodium Hypochlorite → HCID 21386969, compound

https://huagongshe.com/reaction/1834326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 59920066HCID 59920066—
ProductHCID 21386969HCID 21386969—

Reaction Steps

Into a 250 ml 4-neck round bottom flask equipped with a reflux condenser, thermometer, graduated addition funnel and a magnetic stirrer was added 18.1 grams (0.14 moles) of methyl ethyl ketone isopropyl-hydrazone. With efficient stirring 170 mls of 12.4% by wt. aqueous sodium hypochlorite was added dropwise while holding the reaction temperature at 25°-30° C with a water bath. The oxidation was monitored by gas chromatography and after 3 hours stirring the hydrazone was completely oxidized. The reaction mixture was transferred to a separatory funnel and the spent aqueous hypochlorite solution separated. The organic layer was washed with 40 ml of cold 15% sodium bisulfite solution and then 25 ml of sodium bicarbonate solution. The organic layer was taken up in 50 ml of pentane, dried over anhydrous sodium sulfate, filtered and the pentane evaporated on a rotating evaporator under reduced pressure at 10°-20° C. The residue was an orange-yellow liquid weighing 9.4 grams (46.5% crude yield). The infrared spectrum of the product was similar to the infrared spectrum of 2-isopropylazo-2-hydroxybutane prepared by the α-chloro route (Example 5-a-2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04069377
Source datasetuspto-grants-1978_01
ORD IDord-2ebd4242e3e7454f9880e716c892cfb1
Source noteuspto-grants-1978_01