Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262302Generated: October 31, 2026

Diketene → 3-Oxo-N-(2-oxo-2H-benzo[d]imidazol-5-yl)butanamide

https://huagongshe.com/reaction/262302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiketeneHCID 12661—
Reactant5-amino-2H-1,3-benzodiazol-2-oneHCID 15250547—
Reactant5-Acetoacetyl-aminobenzimidazoloneHCID 19356865—
SolventWaterHCID 962—
Product3-Oxo-N-(2-oxo-2H-benzo[d]imidazol-5-yl)butanamideHCID 11776058—

Reaction Conditions

Temperature40 °C

Reaction Steps

Via the bottom inlet tube of a glass vessel having a capacity of 80 liters, a clarified solution of 150 kg of 5-aminobenzimidazolone in 4200 l of water, which solution has a temperature of 90° C., is fed in at a rate of 2100 l/h with agitation. Simultaneously, via a cover inlet tube, diketene is added at a rate of 50 l/h. Immediately, a colorless precipitate of 5-acetoacetyl-aminobenzimidazolone forms. The suspension thus obtained flows via a lateral tube which limits the reaction volume to 40 l into a 8 m3 agitation vessel of stainless steel containing already 1000 l of water having a temperature of 80° C. The reaction temperature in the glass vessel is maintained at 80°-85° C. by spraying water having a temperature of 5° C. onto the surface of the suspension by means of a spray ring (amount of water about 500-600 l/h). After the reaction is complete, the reaction mixture is cooled to 40° C., and the 5-acetoacetylaminobenzimidazolone is isolated by means of a suitable filter. 550 kg of a reaction product of about 40% strength are thus obtained which may be directly used for pigment synthesis without a further purification step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04153798
Source datasetuspto-grants-1979_05
ORD IDord-99fe0648415f4301bec337c331a25962
Source noteuspto-grants-1979_05