Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 22854878 | HCID 22854878 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22854874 | HCID 22854874 | — |
Reaction Steps
3 g of methyl-2-[3-chloro-4-(trans-2-hydroxycyclohexane-1-yl methyl)phenyl]propionate were incorporated with 80 ml of an aqueous methanol containing 1.2 g of sodium hydroxide and then refluxed under heat for two hours. After the end of the reaction, the reaction mixture was treated to concentrate the solvent at a reduced pressure, incorporated with 50 ml of water and washed with 50 ml of ethyl acetate, after which the aqueous layer obtained was adjusted to a pH of 2 with conc. hydrochloric acid. The aqueous layer so adjusted was extracted with 50 ml of ethyl acetate, washed with water, dried and then freed of the solvent to obtain a residue. The thus obtained residue was recrystallized from isopropyl ether thereby to obtain 2.5 g (yield of 2-[3-chloro-4-(trans-2-hydroxycyclohexane-1-yl methyl)phenyl]propionic acid having the following melting point and instrumental analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05434292 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-28d9d3af91d649a589f6ebb141e87e62 |
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| Source note | uspto-grants-1995_07 |
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