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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447355Generated: October 31, 2026

Water → ethyl 4,5-dihydro-4-methyl-5-oxo-3H-1,4-benzodiazepine-2-glyoxylate alpha-oxime

https://huagongshe.com/reaction/1447355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium NitrateHCID 24268—
ReactantHCID 86738265HCID 86738265—
SolventAcetic AcidHCID 176—
Productethyl 4,5-dihydro-4-methyl-5-oxo-3H-1,4-benzodiazepine-2-glyoxylate alpha-oximeHCID 86738266—

Reaction Steps

32.2 g (0.124 mol) of ethyl (1,3,4,5-tetrahydro-4-methyl-5-oxo-2H-1,4-benzodiazepin-2-ylidene)acetate are dissolved in 300 ml of acetic acid and treated at room temperature with 12.8 g (0.186 mol) of sodium nitrate. The mixture is stirred at room temperature for a further 10 minutes, then poured into 1 liter of water and extracted three times with 200 ml of chloroform each time. The combined chloroform phases are washed with 100 ml of water, dried over magnesium sulphate and evaporated. The residue is recrystallised from ethyl acetate. There is obtained ethyl 4,5-dihydro-4-methyl-5-oxo-3H-1,4-benzodiazepine-2-glyoxylate α-oxime of melting point 173°-174° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04316839
Source datasetuspto-grants-1982_02
ORD IDord-903d6b4e0e5e45f7bed80b3543d6571d
Source noteuspto-grants-1982_02