Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromodecane | HCID 8173 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,6-Trihydroxybenzaldehyde | HCID 68099 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86638314 | HCID 86638314 | 88% |
Reaction Steps
A mixture of 2,4,6-trihydroxybenzaldehyde (3.00 g, 19.5 mmol), 1-bromodecane (25.87 g, 117.0 mmol), K2CO3 (8.07 g, 58.4 mmol), and KI (549 mg, 3.3 mmol) in DMF (150 mL) was stirred for 24 h at 110° C. and then one more portion of 1-bromodecane (5.0 g, 22.6 mmol) was added and continued stirring for another 24 h. The reaction mixture was cooled to 20° C. and extracted with CH2Cl2. The organic phase was washed with brine, dried (Na2SO4), and evaporated. Column chromatography (silica gel, hexane/CH2Cl2, 1:1, v/v) afforded the product (9.86 g, 88%) as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993804B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-273fe3a21b334767b1ecf4ebbeb6d73d |
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| Source note | uspto-grants-2015_03 |
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