Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl 5-bromopyridine-3-carboxylate | HCID 140785 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | (5-Bromo-3-pyridinyl)methanol | HCID 2784733 | — |
Reaction Steps
1.1 1.3 g of ethyl 5-bromonicotinate are initially introduced in 40 ml of tert-butanol, and 427 mg of sodium borohydride are added. The entire mixture is heated under reflux (100° C.) and under N2 for one hour. 6 ml of methanol are then added. The mixture is stirred overnight. 10 ml of water is added to the reaction solution. The mixture is then extracted with dichloromethane, dried using sodium sulfate and evaporated in a rotary evaporator, giving 300 mg of (5-bromopyridin-3-yl)methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432282B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-87210240e42b4d9fb76e0e0e05f97748 |
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| Source note | uspto-grants-2008_10 |
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