Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 117599933 | HCID 117599933 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 117599874 | HCID 117599874 | — |
Reaction Steps
3M PhMgBr in diethyl ether (1.7 mL, 5.07 mmol, 1.1 eq.) is added dropwise to the solution of 4-Bromo-2-iodo-3-methyl-benzoic acid ethyl ester (1.7 g, 4.61 mmol), LiCl (195 mg, 4.61 mmol) in dry THF (50 mL) at −10° C. The mixture is stirred at −10° C. for 2 hours. Benzaldehyde (0.977 g, 9.22 mmol) is slowly added to mixture at −10° C. This solution is stirred at room temperature for 16 hours and diluted with saturated aqueous ammonium chloride solution (100 mL). This solution is extracted with ethyl acetate (3×70 mL). The combined organic layers are washed with water and brine, dried over anhydrous sodium sulfate, concentrated in vacuo. The residue is purified by a silica chromatography to give the desire compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102684B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-aaacb8f722bd4237a448338eb9c356eb |
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| Source note | uspto-grants-2015_08 |
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