Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-Fluoro-6-iodobenzoic acid | HCID 2733302 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Trimethyl borate | HCID 8470 | — |
| Product | (2-Fluoro-6-iodophenyl)methanol | HCID 59705003 | — |
Reaction Steps
To a stirred solution of 2-fluoro-6-iodobenzoic acid (10 mmol) in THF (6.5 mL) and trimethylborate (3.25 mL) was added borane dimethylsulfide (12 mmol) slowly, maintaining the internal temperature at 20-25° C. Stirring was continued for an additional 16 h at room temperature and then methanol (1.44 mL) was added cautiously. The resulted solution was evaporated in vacuo to offer 2.5 g of the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884109B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-52199c7415654bbab26adb125b52999e |
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| Source note | uspto-grants-2011_02 |
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