Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromonaphthalene-2,7-diol | HCID 14954841 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66750509 | HCID 66750509 | — |
Reaction Steps
3-Bromonaphthalene-2,7-diol (1.40 g, 5.88 mmol) is dissolved in 20 mL of DMF. Potassium carbonate (2.44 g, 17.6 mmol) is added and the mixture is heated to 60° C. Benzyl bromide (2.10 mL, 17.64 mmol) is added and heating is continued for 5 h, after which time the reaction is poured into water and extracted with MTBE. The combined organics are dried and evaporated to afford 3,6-bis-benzyloxy-2-bromonaphthalene as a brown solid, which is of sufficient purity to take on to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700633B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-9bc902bb8e1a4ee89f1291322d11b0f2 |
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| Source note | uspto-grants-2010_04 |
|---|