Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 22595687 | HCID 22595687 | — |
| Solvent | Piperidine | HCID 8082 | — |
| Product | 4-(Methanesulfinyl)benzaldehyde | HCID 3015943 | — |
Reaction Steps
220 mg of 2-[4-(3-chloro-1-thiapropyl)-phenyl]-7-hydroxy-3-(4-hydroxyphenyl)-4-(trifluoromethyl)-2H-1-benzopyran in 2 ml of piperidine is mixed with 42.7 mg of potassium iodide and stirred for 6 hours at 100° C. After cooling, it is poured into water and shaken out three times with ethyl acetate. The combined organic phases are washed twice with water, dried on magnesium sulfate and concentrated by evaporation in a rotary evaporator. The purification of the product is carried out on silica gel with dichloromethane/methanol-9:1. 274 mg of product accumulates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06844336B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-72cc06068bd54f58907552f582fca3d1 |
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| Source note | uspto-grants-2005_01 |
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