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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238178Generated: October 30, 2026

Water → 2-phenyl-5,6-dihydro-4H-1,3,4-oxadiazin-5-one

https://huagongshe.com/reaction/238178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
Reactantn'-(2-Chloroacetyl)benzohydrazideHCID 736972—
ReactantDichloromethane ethylacetateHCID 21226138—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-phenyl-5,6-dihydro-4H-1,3,4-oxadiazin-5-oneHCID 14203474—

Reaction Conditions

Temperature100 °C

Reaction Steps

812 g (3.82 mol) of N′-(2-chloroacetyl)benzenecarbohydrazide were dissolved in 13 liters of dry DMF, and 384.95 g (4.58 mol) of sodium bicarbonate were added. The reaction solution was then heated to 100° C. and stirred at this temperature overnight. After the reaction had gone to completion (monitored by TLC, mobile phase dichloromethane/ethyl acetate 9:1), the reaction solution was cooled to room temperature, poured into 65 liters of water and extracted three times with in each case 17.5 liters of ethyl acetate. The combined organic phases were washed with 13.8 liters of saturated aqueous sodium bicarbonate solution, dried and concentrated to dryness under reduced pressure. The solid obtained was dissolved in a 9:1 mixture of dichloromethane and methanol and applied to 17 kg of silica gel. Using two portions of silica gel (8 kg each), the product was chromatographed using 260 liters of dichloromethane/ethyl acetate 9:1 as mobile phase. The combined product fractions were concentrated, and the resulting solid was triturated with 3 liters of diethyl ether. Filtration gave 247 g (1.40 mol, 35% of theory) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642592B2
Source datasetuspto-grants-2014_02
ORD IDord-b0d713fb7a144300be4a5e9175bee46e
Source noteuspto-grants-2014_02