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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765856Generated: October 25, 2026

Water → 3-Bromo-5-tert-butyl-6-isopropoxy-2-methyl-benzaldehyde

https://huagongshe.com/reaction/1765856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsopropyl iodideHCID 6362—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromo-5-tert-butyl-6-hydroxy-2-methyl-benzaldehydeHCID 21107150—
SolventDimethylformamideHCID 6228—
Product3-Bromo-5-tert-butyl-6-isopropoxy-2-methyl-benzaldehydeHCID 2110715164.1%

Reaction Conditions

Temperature75 °C

Reaction Steps

A stirred, cooled (ice bath) solution of 3-bromo-5-tert-butyl-6-hydroxy-2-methyl-benzaldehyde (Intermediate 140, 0.58 g, 2.14 mmol) in anhydrous N,N-dimethylformamide (10 mL) was treated with sodium hydride (0.34 g of 60% suspension in mineral oil, 8.56 mmol). After 30 minutes, 2-iodopropane (1.3 mL, 12.84 mmol) was added and the reaction mixture was heated at 75° C. overnight. The reaction mixture was then cooled and poured into iced water and extracted with diethyl ether. The organic extract was then washed with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to an oil. Flash column chromatography using 2–4% ethyl acetate in hexane as the eluent afforded the title product (0.43 g, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226951B2
Source datasetuspto-grants-2007_06
ORD IDord-1885004ad5d54ce99753ccca2eb07dc8
Source noteuspto-grants-2007_06