Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 86759278 | HCID 86759278 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86759277 | HCID 86759277 | — |
Reaction Steps
To a reaction mixture containing the (Z)-styryl 2-hydroxyphenylsulfide (5 mmol), anhydrous pyridine (5 mmol) and acetic anhydride (5 mmol) in dry chloroform (10 ml) is stirred for 5 hours at room temperature (22° C.). The reaction mixture is then diluted with water (20 ml) and shaken well in a separating funnel. The lower organic layer is collected and dried over anhydrous sodium sulfate. Evaporation of the chloroform in vacuum yields the corresponding (Z)-styryl 2-acetoxyphenylsulfide (I) as an oil, or in most cases a colorless solid. The products are purified by TLC or by fractional crystallization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06656968B1 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-39ffca204c614dd78144203a1ff38717 |
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| Source note | uspto-grants-2003_12 |
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