HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501780Generated: October 30, 2026
Hydrochloric Acid → HCID 178447588, compound
https://huagongshe.com/reaction/501780
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 68457984 | HCID 68457984 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178447588 | HCID 178447588 | 58.7% |
Reaction Steps
1.02 g of {[3-(5-[4-(cyclopentyloxy)-2-hydroxybenzoyl]-2-{[3-(methoxymethoxy)-1,2-benzisoxazol-6-yl]methoxy}phenyl) propanoyl]oxy}methyl pivalate was dissolved in 8 mL of 1,4-dioxane and 8 mL of methanol, to which 6 mL of 6M hydrochloric acid was added at room temperature, and this mixture was stirred for 50 minutes at the same temperature. The reaction mixture, to which water was added, was adjusted to pH 7 with an aqueous solution of sodium hydroxide, and then ethyl acetate was added to this mixture and the organic phase was separated therefrom. The remaining aqueous phase was extracted with ethyl acetate, and organic phases were combined together. After the resultant organic phase was washed with a saturated sodium chloride solution, the washed phase was dried over anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure. The resultant residue, to which a mixture of hexane and ethyl acetate [3:1] was added, was filtered out to yield 0.56 g of [(3-{5-[4-(cyclopentyloxy)-2-hydroxybenzoyl]-2-[(3-hydroxy-1,2-benzisoxazol-6-yl)methoxy]phenyl} propanoyl)oxy]methyl pivalate as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772285B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-a89867fae65e454e854eb1fe8a4cd9fd |
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| Source note | uspto-grants-2010_08 |
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