HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41241Generated: October 28, 2026
Toluene → (3-Chloro-4-iodo-5-methoxyphenyl)methanol
https://huagongshe.com/reaction/41241
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Ethyl 3-chloro-4-iodo-5-methoxybenzoate | HCID 57912451 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3-Chloro-4-iodo-5-methoxyphenyl)methanol | HCID 57912436 | 100% |
Reaction Steps
To a mixture of ethyl 3-chloro-4-iodo-5-methoxybenzoate (15.6 g, 45.8 mmol) and toluene (150 mL), was added diisobutyl aluminum hydride (1.01M toluene solution: 95.2 mL, 96.2 mmol) while stirring at −78° C., and the mixture was stirred while warming to −30° C. for three hours. To the mixture, an aqueous solution (400 mL) of Rochelle salt (potassium sodium (+)-tartrate tetrahydrate) (77.6 g, 275 mmol) was added, the mixture was stirred at room temperature for five hours, followed by addition of ethyl acetate. After thoroughly shaking the mixture, the organic layer was separated, and the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The mixture was filtered, and then the solvent in the filtrate was distilled off under reduced pressure to obtain the title compound (13.7 g, 45.8 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530504B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-1bbe67e71f234738a46e25bab67a2b00 |
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| Source note | uspto-grants-2013_09 |
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