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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Bromo-5-tert-butyl-6-hydroxy-2-methyl-benzaldehyde | HCID 21107150 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Bromo-5-tert-butyl-6-isopropoxy-2-methyl-benzaldehyde | HCID 21107151 | 64.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07226951B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-1885004ad5d54ce99753ccca2eb07dc8 |
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| Source note | uspto-grants-2007_06 |
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