Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 86623630 | HCID 86623630 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68852261 | HCID 68852261 | — |
Reaction Steps
Ethyl (4-(5-(3-cyano-4-(2-propyloxy)phenyl)-thien-2-yl)-3-methylphenyl)propanoate (from STEP E) was combined with 200 mg of lithium hydroxide, 3 mL of tetrahydrofuran and 1 mL of water. The reaction mixture was heated to 55° C. for 6 h, combined with 50 mL of ethyl acetate, 50 mL of 1 M solution of hydrochloric acid. The organic layer was separated, washed with brine, dried over sodium sulfate and concentrated. The title compound was isolated by flash chromatography on silica gel using 10% methanol in dichloromethane as the eluant: 1H NMR (CDCl3) 7.81 (d, J=2.0, 1H), 7.74 (dd, J=2.0, 9.0, 1H), 7.38 (d, J=8.0, 1H), 7.22 (d, J=4.0, 1H), 7.16 (d, J=1.0, 1H), 7.11 (dd, J=1.0, 8.0, 1H), 7.03 (d, J=4.0, 1H), 7.00 (d, J=8.0, 1H), 4.70 (sep, J=1.0, 1H), 3.00 (t, J=1.5, 2H), 2.75 (t, J=1.5, 2H), 2.47 (s, 3H), 1.42 (d, J=1.0, 6H); HPLC A 3.78 min; ESI-MS (m/z)=406.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605171B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-91e1b0f76b894f2cbc022d9ecf332285 |
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| Source note | uspto-grants-2009_10 |
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