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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425053Generated: October 31, 2026

N-bromobutanimide → HCID 57684692, compound

https://huagongshe.com/reaction/425053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 57684693HCID 57684693—
SolventChlorobenzeneHCID 7964—
ProductHCID 57684692HCID 57684692—

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of (2R,3R,4R,5S,6S)-2-(acetoxymethyl)-6-(4-chloro-3-(4-(prop-1-en-2-yl) benzyl)phenyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate (intermediate AZ) (236 mg, 0.412 mmol) and NBS (110 mg, 0.618 mmol) in chlorobenzene (5 mL) was stirred at 135° C. for 2 h. The solids were filtered and washed with AcOEt. The organic portion was washed 1× with H2O and 1× with brine prior to drying over Na2SO4. Concentration and purification of the resulting residue by preparative TLC gave intermediate AZ (144 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106021B2
Source datasetuspto-grants-2012_01
ORD IDord-6c61171ae130434db439a7fed9017977
Source noteuspto-grants-2012_01