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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731140Generated: November 3, 2026

Triethyloxonium tetrafluoroborate → HCID 21495341, compound

https://huagongshe.com/reaction/1731140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
ReactantHCID 21495275HCID 21495275—
SolventDichloromethaneHCID 6344—
ProductHCID 21495341HCID 21495341—

Reaction Steps

A solution of triethyloxonium fluoroborate (3.5 g) and the amide of formula X, N,1-dimethyl-1,3,4,9-tetrahydroindeno[2,1-c]pyran-1-propionamide (5.5 g), described in Example 108, in 100 ml of methylene chloride is evaporated at reduced pressure and the residue dissolved in 50 ml of absolute ethanol. Sodium borohydride (1.35 g) is added in portions to the stirred solution at 0° C. When the addition is complete, stirring is continued for 18 hr. at 25° C. The solution is poured into 250 ml of water and extracted with 3 × 30 ml portions of ether. The combined extracts are washed with water, dried (MgSO4) and evaporated yielding the title compound, identical to the product of Example 285.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03995052
Source datasetuspto-grants-1976_11
ORD IDord-5042efa4ccc6488a8422fc4bf2e32da5
Source noteuspto-grants-1976_11