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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597701Generated: October 29, 2026

Hexanal → HCID 131710289, compound

https://huagongshe.com/reaction/597701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexanalHCID 6184—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 131710289HCID 13171028937%

Reaction Steps

24.5 g (0.05 M) of 4-bromo-pent-2trans-en-1-yl triphenylphosphonium bromide [which can be prepared according to the above given procedure] were slowly added to a suspension kept under stirring and in argon atmosphere of 13.5 g (0.12 M) of potassium ter-butoxide in 100 ml of anhydrous ether. The reaction mixture was kept under stirring overnight, whereupon 5 g (0.05 M) of hexanal in 35 ml of anhydrous ether were added thereto at a temperature of ca. 15°-25°. After having been left at 35° for 1 h, the mixture was cooled to room temperature, diluted with 130 ml of hexane, filtered over Celite and the clear filtrate, after washing with a saturated aqueous solution of NH4Cl and drying over magnesium sulphate, was kept 1 day at -20°. A subsequent purification was carried out by column chromatography by using 100 g of silica gel and elution with hexane. By distillation of the residue obtained on evaporation of the volatile portion of the eluate, 2.8 g (37 %) of a mixture comprising 44:56 parts by weight of hydrocarbons Ic and Id was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014951
Source datasetuspto-grants-1977_03
ORD IDord-761edb82722343f1aaa8c7b1fbc4df24
Source noteuspto-grants-1977_03