HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894828Generated: October 31, 2026
Hydrochloric Acid → (3-Butoxy-4-iodophenyl)methanol
https://huagongshe.com/reaction/1894828
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Methyl 3-butoxy-4-iodobenzoate | HCID 59574927 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Butoxy-4-iodophenyl)methanol | HCID 59574926 | 100.1% |
Reaction Steps
8.17 g (0.375 mol, 3 eq) of lithium borohydride are added to a solution of 41.78 g (0.125 mol, 1 eq) of methyl 3-butoxy-4-iodobenzoate in 210 ml of tetrahydrofuran. The reaction medium is heated at 60° C. for 2 hours and then hydrolyzed cautiously with ice-cold saturated ammonium chloride solution. The reaction medium is neutralized with concentrated hydrochloric acid and then extracted with ethyl acetate. The organic phases are washed with water and dried over magnesium sulfate. The solvent is evaporated off to give 38.31 g of (3-butoxy-4-iodophenyl)methanol in the form of a whitish oil. Yield=100%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513297B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-186b767bec944029b3ea1ae900e5ee76 |
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| Source note | uspto-grants-2013_08 |
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