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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904835Generated: October 30, 2026

N-bromobutanimide → HCID 53640973, compound

https://huagongshe.com/reaction/904835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 20477712HCID 20477712—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53640973HCID 5364097330%

Reaction Steps

To a stirred solution of 1.6 g. (5 mM) of 1-(thiazolin-2-yl)-2-amino-6-(α-methylenebenzyl)benzimidazole in 150 ml. of tetrahydrofuran were added in one portion 900 mg. (0.5 mM) of N-bromosuccinimide. The reaction mixture was stirred at room temperature for seventy-two hours, and then was concentrated to a volume of about 10 ml. by evaporation of the solvent under reduced pressure. The reaction mixture was diluted with 20 ml. of water, and the crystalline precipitate that formed was collected by filtration and identified as 600 mg. of 1-(thiazolin-2-yl)-2-amino-6-(α-bromomethylenebenzyl)benzimidazole. M.P. 197°-199° C. Yield 30%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04420479
Source datasetuspto-grants-1983_12
ORD IDord-12c91b8260ff46f1b0dc9265a0044ddc
Source noteuspto-grants-1983_12