Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(1,1-Dimethyl-3-trifluoromethyl-3-trimethylsilanyloxyhex-5-ynyl)benzoic acid | HCID 58026143 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58026145 | HCID 58026145 | 44% |
Reaction Steps
To a solution of 2-(1,1-dimethyl-3-trifluoromethyl-3-trimethylsilanyloxyhex-5-ynyl)benzoic acid (246 mg, 0.64 mmol) in 5 mL of dichloromethane was added pyridine (77 μL, 0.96 mmol) followed by thionyl chloride (56 μL, 0.76 mmol). The reaction was stirred for 15 minutes then the volatiles were removed in vacuo. The crude acid chloride was treated with 7 M ammonia in 5.0 mL of MeOH. The mixture was stirred for 15 minutes then diluted with 75 mL of EtOAc, washed with two 25 mL portions of saturated aqueous sodium bicarbonate solution, dried over magnesium sulfate, filtered, and concentrated in vacuo. Purification of the crude by flash chromatography (12 g SiO2, hexanes to 1:1 hexanes:EtOAc) gave 2-(1,1-dimethyl-3-trifluoromethyl-3-trimethylsilanyloxyhex-5-ynyl)benzamide as a pale yellow solid (108 mg, 44%). MS (ES+) m/z 386 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268859B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-fac19b4586474ebabb2743b107f4b43d |
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| Source note | uspto-grants-2012_09 |
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