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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28171Generated: October 26, 2026

Hydroxylamine → 3,4-Dichlorobenzylthioaceto-hydroxamic acid

https://huagongshe.com/reaction/28171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantSulfuric AcidHCID 1118—
Reactant1,1-DichloroethaneHCID 6365—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178526174HCID 178526174—
SolventMethanolHCID 887—
Product3,4-Dichlorobenzylthioaceto-hydroxamic acidHCID 8673610175%

Reaction Steps

20.2 g (0.08 mol) of 3,4-dichlorobenzylthioacetic acid are esterified with 10 ml of methanol, 0.6 ml of concentrated H2SO4 and 100 ml of dichloroethane. The mixture is heated under reflux for 4 hours, washed with water and with dilute bicarbonate solution, and dried. The mixture is evaporated in vacuo. The oily residue, in methanol, is treated with a solution of hydroxylamine (0.1 mol) in the presence of 0.18 mol of sodium methylate. After leaving the reactants in contact overnight, the mixture is evaporated to dryness in vacuo, the residue is taken up in water, the mixture is filtered over charcoal and the filtrate is precipitated with 3N HCl, the product is extracted with ether, the extract is dried and evaporated and the product is crystallised in diisopropyl ether. 15 g of the stated product are obtained (yield 71%). Melting point: 75°-76° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04225617
Source datasetuspto-grants-1980_09
ORD IDord-a0204dc1ec8643429653b00bdfa853c5
Source noteuspto-grants-1980_09