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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280257Generated: November 2, 2026

Isobutylene → chloroacetaldehyde O-tert-butyloxime

https://huagongshe.com/reaction/1280257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(2-Chloroethylidene)hydroxylamineHCID 57350373—
SolventDiethyl EtherHCID 3283—
Productchloroacetaldehyde O-tert-butyloximeHCID 53697151—

Reaction Steps

Then, 0.47 g of chloroacetoaldehyde oxime, 0.1 ml of concentrated sulflic acid, and 10 ml of diethyl ether are placed in a reaction vessel, into which isobutene gas is blown with stirring under ice cooling, and the stirring is further continued at room temperature. After completion of the reaction, the reaction mixture is slowly poured into saturated aqueous sodium hydrogencarbonate solution, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with 10% aqueous sodium hydroxide solution and water in this order, dried over anhydrous magnesium sulfate, and concentrated, which affords chloroacetoaldehyde O-tert-butyloxime.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448444B1
Source datasetuspto-grants-2002_09
ORD IDord-6fe1b3a8e39f41808b795413f2455f89
Source noteuspto-grants-2002_09