HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770128Generated: November 1, 2026
3-Hydroxybenzoic Acid → HCID 15225618, compound
https://huagongshe.com/reaction/1770128
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxybenzoic Acid | HCID 7420 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | alpha-Cyclohexylcyclohexanemethanol | HCID 78197 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 15225618 | HCID 15225618 | 18% |
Reaction Steps
To a solution of 3-hydroxybenzoic acid (1.61 g, 8.2 mmol), dicyclohexylmethanol (1.61 g, 8.2 mmol), triphenylphosphine (2.05 g, 7.82 mmol) and dioxane (35 ml) was added diethyl azodicarboxylate (1.41 ml, 8.94 mmol), and the resultant mixture was refluxed for 3 days. The reaction mixture was allowed to warm up to room temperature, poured into chilled water and extracted with diethyl ether. The organic layer was concentrated, and the residue was dissolved in a mixture of methanol (20 ml), tetrahydrofuran (6.5 ml) and water (2.0 ml), mixed with potassium hydroxide (1.16 g) and stirred for 2 hours. The mixture was poured into chilled water, acidified, and extracted with ethyl acetate. The organic layer was concentrated, and the resultant residue was recrystallized from hexane to give the titled compound (0.43 g, yield 18%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05385917 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-d90969d5d77d4293bc01a73a9a256904 |
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| Source note | uspto-grants-1995_01 |
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