HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 84013601, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Furo[2,3-b]pyridine-3-carbaldehyde | HCID 21794742 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 84013601 | HCID 84013601 | — |
Reaction Steps
To a suspension of furo[2,3-b]pyridine-3-carboxaldehyde (67 mmol) [J. Heterocyclic Chem., 23, 1465 (1986)] in 52 mL H2O were added NaH2PO4 (67 mmol), 260 mL t-BuOH, 71 mL 2-methyl-2-butene followed by portionwise addition of NaClO2 (100 mmol) at 0° C. After 15 min, the cooling bath was removed and the reaction was stirred at RT for 24 h. A solution of sat. aq. NaHCO3 was added and the mixture was extracted with EtOAc. The water phase was acidified with 1N HCl solution and it was then extracted 3 times with EtOAc. The combined organic layers were dried over MgSO4 and concentrated in vacuo to obtain the desired compound as beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409917B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-07584ecf2af24ffcb984e42830f28cf5 |
| Source note | uspto-grants-2016_08 |