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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734629Generated: October 31, 2026

N-bromobutanimide → HCID 54404171, compound

https://huagongshe.com/reaction/1734629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 54044812HCID 54044812—
SolventDimethylformamideHCID 6228—
ProductHCID 54404171HCID 54404171—

Reaction Steps

(±)-(1R*, 2S*, 3S*, 5S*)-3-(Acetoxymethyl)-5-(5,6-dichloro-1H-benzimidazol-1-yl)-1,2-cyclopentanediyl diacetate (1.32 g, 2.98 mmol) in dry N, N-dimethylformamide (6 mL) was heated to 60° C. Portions (ca. 1 mmol each) of N-bromosuccinimide (1.59 g, 8.93 mmol) were added over 5 hours. Heating was continued for an additional 4 hours. Volatiles were removed in vacuo and the residue chromatographed on silica gel. Title compound eluted with 1:1 hexane-ethylacetate as a tan powder (1.1 g, 69%), 1H-NMR identical with recrystallized sample. Such a sample was recrystallized from ethanol-water to a white powder, m.p. 156°-159° C.; 1H-NMR (DMSO-d6)δ: 8.34, 7.97 (both s, 1 each, 2 benzimidazole CH), 5.6 (m, 1, OCH), 5.3 (m, 1, OCH), 5.2-5.0 (m, 1, NCH), 4.4-4.2 (m, 2, OCH2), 2.7-2.5 (m, 1, CH), 2.4-2.0 (m) overlapping 2.1 and 2.07 (both s, total 8, CH2 and 2CH3CO), 1.92 (s, 3, CH3CO); mass spectrum (CI): 527 (6.6), 525 (45), 523 (100), 521 (65, M+1), 257 (48, M-B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534535
Source datasetuspto-grants-1996_07
ORD IDord-fb2d5fb684034bf6a3d8bae83f806169
Source noteuspto-grants-1996_07