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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897372Generated: October 30, 2026

N-bromobutanimide → HCID 16753950, compound

https://huagongshe.com/reaction/897372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 16753949HCID 16753949—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 16753950HCID 16753950—

Reaction Steps

A mixture of 5-fluoro-N,N,2-trimethylbenzenesulfonamide (5.20 g, 24.0 mmol) and N-bromosuccinimide (4.69 g, 26.4 mmol) in dry CCl4 (100 mL) was refluxed overnight under nitrogen. Cooled the reaction and filtered off the succinimide salts by vacuum filtration, washing with CCl4. The concentrated filtrate was dissolved in a minimal amount of ethyl acetate and purified on an Isco column (110 g silica) running a 0 to 20% EtOAc/Hexane gradient over 40 minutes. The collected fractions were concentrated in vacuo to afford the desired material as a yellow oil in a ratio of 3.5:1 with the starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921759B2
Source datasetuspto-grants-2005_07
ORD IDord-d8f7aac57dcb4d8fb5b0dbdb7782523a
Source noteuspto-grants-2005_07