HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249616Generated: November 2, 2026
Hydrochloric Acid → 2-{5-[(2,4-Diisobutoxyphenyl)(hydroxy)methyl]-2-isobutoxyphenyl}-acetic acid
https://huagongshe.com/reaction/2249616
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-[5-(2,4-Diisobutoxybenzoyl)-2-isobutoxyphenyl]acetic acid | HCID 17816564 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-{5-[(2,4-Diisobutoxyphenyl)(hydroxy)methyl]-2-isobutoxyphenyl}-acetic acid | HCID 57684380 | 49.8% |
Reaction Steps
In 2 ml of methanol is dissolved 100 mg of 2-[5-(2,4-diisobutoxybenzoyl)-2-isobutoxyphenyl]acetic acid. After adding 18 mg of sodium borohydride at 5-10° C., the mixture thus obtained is stirred at 50-60° C. for one hour. Then, 40 mg of sodium borohydride and 40 mg of lithium chloride are further added at ambient temperature, and the mixture thus obtained is stirred at 50-60° C. for two hours. Chloroform and water are added to the reaction mixture, pH is adjusted to 2.0 with 2 mol/L hydrochloric acid, and the organic layer is separated. The organic layer is successively washed with water and saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. Thus, 50 mg of 2-{5-[(2,4-diisobutoxyphenyl)(hydroxy)methyl]-2-isobutoxyphenyl}-acetic acid is obtained as a colorless oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314888B1 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-4925ea3363ae4cd391512edc94ca8433 |
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| Source note | uspto-grants-2008_01 |
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