Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 21964303 | HCID 21964303 | — |
| Product | HCID 10142972 | HCID 10142972 | — |
Reaction Steps
Oxalyl chloride (1.05 mL) was added dropwise to a stirring solution of {1-(4-methylbenzyl) -5-[4-(trifluoromethoxy)phenyl]-1H-indol-2-yl}methyl acetate (0.515 g) in THF (17 mL) at room temperature over a period of 5 minutes under a nitrogen atmosphere. After the reaction mixture was stirred at room temperature for 4 hours, the reaction was quenched carefully with water. The aqueous mixture was extracted with ethyl acetate. The extract was washed with water, and brine, dried over anhydrous magnesium sulfate, and concentrated to give the title compound as a light brown solid, mp: 79-80° C. Mass spectrum (ESI, [M−H]−) m/z 524. 1HNMR (400 MHz, DMSO-d6): δ 14.50 (br s, 1H), 8.20 (s, 1H), 7.74 (d, 2H, J=8.55 Hz), 7.70 (d, 1H, J=8.69 Hz), 7.62 (d, 1H, J=8.55 Hz), 7.47 (d, 2H, J=8.25 Hz), 7.15 (d, 2H, J =7.88 Hz), 6.99 (d, 2H, J=7.78 Hz), 5.64 (s, 2H), 5.53 (s, 2H), 2.25 (s, 3H), and 1.83 ppm (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07459478B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-7cf5267b8c9c4c39b59e9316bcac1df1 |
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| Source note | uspto-grants-2008_12 |
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