Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481316Generated: November 1, 2026

tert-Butanol → HCID 84013601, compound

https://huagongshe.com/reaction/1481316

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantFuro[2,3-b]pyridine-3-carbaldehydeHCID 21794742—
ReactantSodium ChloriteHCID 23668197—
SolventWaterHCID 962—
ProductHCID 84013601HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409917B2
Source datasetuspto-grants-2016_08
ORD IDord-07584ecf2af24ffcb984e42830f28cf5
Source noteuspto-grants-2016_08