Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 10053169 | HCID 10053169 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11756838 | HCID 11756838 | — |
Reaction Steps
{4-[3,3-Bis-(4-bromo-phenyl)-allyloxy]-2-methyl-phenoxy}-acetic acid methyl ester (1.9 g, 3.5 mmol) was dissolved in warm ethanol (100 ml). 1N NaOH (7 ml, 7 mmol) was added and the reaction mixture was stirred for 2 h at 60° C. after which it was evaporated. The residue was treated with water (50 ml) and 1N HCl (8 ml) and extracted with dichloromethane (2×250 ml). The combined organic phases were dried and evaporated to give the title compound in 1.8 g (99%) yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129268B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-f0ea411f7cf94d25b7e1cd50a64e3dbb |
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| Source note | uspto-grants-2006_10 |
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