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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6208Generated: October 26, 2026

Sodium Chloride → HCID 54151230, compound

https://huagongshe.com/reaction/6208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantTributyl(1,3-dioxolan-2-ylmethyl)phosphonium BromideHCID 22292430—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 54260784HCID 54260784—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 54151230HCID 54151230—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution 30.3 g (0.1 mole) of N-acetoxyhexyl-1,2,3,4-tetrahydroquinoline-6-carboxaldehyde in dimethylformamide is added 7.4 g (0.2 mole) of 1,3-dioxolan-2-ylmethyltributylphosphonium bromide in dimethylformamide with magnetic stirring, and the mixture is heated at 90° C. Potassium t-butoxide (22.4 g, 0.2 mole) is added, and heating is continued at 90° C. for 16 hours. After cooling to room temperature, the solution is poured into a seven-fold excess of water. The aqueous mixture is saturated with sodium chloride, and the mixture is extracted with three portions of ether. The combined organics are dried over 4A sieves, filtered through cotton, and evaporated. The crude reaction product is then dissolved in 3M HCl, and the reaction is stirred at room temperature for 16 hours. After careful neutralization with saturated sodium bicarbonate, the aqueous mixture is extracted with three portions of ether, and the combined organics are passed through silica gel, dried over 4A sieves, filtered through cotton, and evaporated to yield 3-(N-hydroxyhexyl-1,2,3,4-tetrahydroquinolin-6-yl)acrolein.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05247042
Source datasetuspto-grants-1993_09
ORD IDord-f11fb9357654407f897a52ae5b73be5e
Source noteuspto-grants-1993_09