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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273743Generated: October 31, 2026

N-bromobutanimide → HCID 20094251, compound

https://huagongshe.com/reaction/273743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-(5-methylbenzoxazol-2-yl)benzoateHCID 20094237—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 20094251HCID 2009425150.7%

Reaction Steps

N-Bromosuccinimide (2.35 g) and azo(bisisobutyronitrile) (60 mg) were added to a solution of compound C (3.2 g) in carbon tetrachloride (60 ml). The mixture was heated under reflux for 4 hours and then cooled to ambient temperature. Insoluble material was removed by filtration and the filtrate was concentrated. The residue was recrystallised from hexane to give methyl 2-(5-bromomethyl-benzoxazol-2-yl)benzoate (D) (2.1 g), m.p. 92°-95° C; NMR: 3.9(s, 3H), 4.65(s, 2H), 7.45(dd, 1H), 7.55(dd, 1H), 7.6-7.7(m, 2H), 7.8-7.85(m, 2H), 8.0-8.1(m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387592
Source datasetuspto-grants-1995_02
ORD IDord-0f65ea37a79a405892882b27fe8a9fc5
Source noteuspto-grants-1995_02