Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | HCID 66919101 | HCID 66919101 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66919040 | HCID 66919040 | 83.1% |
Reaction Steps
To a solution of (1R,2R)-4-(2-Chloro-benzenesulfonyl)-2-(4-chloro-phenoxymethyl)-cyclopentanecarboxylic acid ethyl ester (epimeric mixture, 132 mg) in tetrandrofuran (2.4 mL), methanol (0.6 mL) and water (1.2 mL) was added lithium hydroxide monohydrate (14 mg). The mixture was stirred at 80° C. for 2.5 h then concentrated in vacuo. The residue was dissolved in water and the pH was adjusted to 1 with hydrochloric acid (2N). The precipitate was filtered, washed with water and dried in vacuo to afford the title compound (103 mg, 83%) as a white solid. MS (EI): 446.1 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893099B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-ce552541e64648e59d9f77ee6bfeadbb |
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| Source note | uspto-grants-2011_02 |
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