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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530135Generated: October 26, 2026

N-bromobutanimide → HCID 58095216, compound

https://huagongshe.com/reaction/1530135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactantbeta-CyclodextrinHCID 444041—
ReactantThioureaHCID 2723790—
Reactant3-(2,4-Dichlorophenyl)-3-oxopropanenitrileHCID 13630728—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 58095216HCID 5809521642%

Reaction Conditions

Temperature50 °C

Reaction Steps

beta-Cyclodextrin (4.29 g, 3.78 mmol) was dissolved in water (75 mL) at 50° C. and a solution of 3-(2,4-dichlorophenyl)-3-oxopropanenitrile (810 mg, 3.8 mmol) in Acetone (3.80 mL) was added dropwise, followed by NBS (0.808 g, 4.54 mmol) and thiourea (0.346 g, 4.54 mmol). Reaction mixture was stirred at 50° C. 1 hr. LCMS indicated complete conversion. Reaction mixture was cooled to rt, extracted with ethyl acetate (3×50 mL), dried with MgSO4, filtered and concentrated under reduced pressure. The residue was purified by ISCO with 5-30% ethyl acetate in hexanes to give 0.43 g of the title compound (42%). LCMS; (FA) ES+, 270, 272, 1H NMR (400 MHz, d1-chloroform) δ 7.49 (d, J=1.84 Hz, 1H), 7.41 (d, J=8.30 Hz, 1H), 7.31 (dd, J=8.16, 1.74 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090601B2
Source datasetuspto-grants-2015_07
ORD IDord-91725012d7174cc38e98f48532a2f06c
Source noteuspto-grants-2015_07