Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372043Generated: October 26, 2026

Sulfuric Acid → 7-(Oxan-2-yloxy)heptanal

https://huagongshe.com/reaction/372043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant7-(2-Tetrahydropyranyloxy)heptanenitrileHCID 20542932—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Product7-(Oxan-2-yloxy)heptanalHCID 182184—

Reaction Conditions

Temperature10 °C

Reaction Steps

Diisobutylaluminium hydride (19.4 g.) in dry benzene (50 ml.) was added dropwise at 10° C. to a stirred solution of 7-(2-tetrahydropyranyloxy)heptanenitrile (20.6 g.) in dry diethyl ether (200 ml.). The solution was stirred at 10° C. for 30 minutes and was then added to 2N aqueous sulphuric acid (300 ml.) at 0° C. The mixture was heated at 30° C. for 30 minutes, and then saturated with sodium chloride and the layers were separated. The aqueous layer was extracted with diethyl ether and the combined organic layers were washed with aqueous sodium bicarbonate, and then aqueous sodium chloride, and dried over sodium sulphate. The solvent was evaporated and the residue was distilled under reduced pressure to give 7-(2-tetrahydropyranyloxy)heptanal (12.7 g.), b.p. 78°-106° C./0.1 mm.Hg, nD25 1.456.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04088695
Source datasetuspto-grants-1978_05
ORD IDord-5d85603004c44d74b1488ebff4d7a1ac
Source noteuspto-grants-1978_05