Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390861Generated: October 30, 2026

N-bromobutanimide → (2-Bromo-4-tert-butyl-5-methoxy-phenyl)-methanol

https://huagongshe.com/reaction/2390861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1206775-43-0HCID 53401457—
SolventCarbon TetrachlorideHCID 5943—
SolventSodium BisulfiteHCID 23665763—
Product(2-Bromo-4-tert-butyl-5-methoxy-phenyl)-methanolHCID 67070042100%

Reaction Steps

step b—To a solution of 345 (2.08 g, 10.70 mmol) in CCl4 (75 mL) was added NBS (2.10 g, 11.80 mmol). The reaction was stirred for 15 min then diluted with a cold 10% aqueous NaHSO3. The reaction mixture was extracted with DCM. The organic extract was washed with brine, dried (MgSO4), filtered and concentrated. The residue was taken up in hexanes (80 mL) and then concentrated to afford 2.9 g (100%) of 344a as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273773B2
Source datasetuspto-grants-2012_09
ORD IDord-1e744d1e0f6d4be5a7ac2ddaf8c8ce87
Source noteuspto-grants-2012_09