Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 59331233 | HCID 59331233 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59331529 | HCID 59331529 | 90.5% |
Reaction Steps
To a solution of methyl 2-[4-(methylsulfonyl)phenyl]-3-(tetrahydrofuran-3-yl)propanoate (3.61 g) in a mixed solvent of methanol (46 mL) was added 2M aqueous sodium hydroxide solution (11.6 mL), and the mixture was stirred at 50° C. for 16 hr. The reaction mixture was acidified with 6M hydrochloric acid, and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give the title compound (3.12 g, 90%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318746B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-8075f1d41c754054b5631d219acc68c9 |
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| Source note | uspto-grants-2012_11 |
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