HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(6-Bromopyridin-3-yl)propan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Ethyl 3-(6-bromopyridin-3-yl)propanoate | HCID 86251977 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(6-Bromopyridin-3-yl)propan-1-ol | HCID 70700830 | — |
Reaction Steps
Under argon, 560 mg (2.17 mmol) of 3-(6-bromopyridin-3-yl)propionic acid ethyl ester and 94.6 mg (4.34 mmol) of lithium borohydride were stirred in 40 ml of THF at 40° C. for 3 h. After cooling, the mixture was cautiously hydrolyzed with water, the precipitate was filtered off with suction, and the filtrate was concentrated and admixed with water and ethyl acetate. The organic phase was separated, washed with water and concentrated. Yield: 450 mg (96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518976B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-9aeda3ff500d435aa60fa387cec9ee18 |
| Source note | uspto-grants-2013_08 |