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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330610Generated: October 30, 2026

Hydrochloric Acid → HCID 14750110, compound

https://huagongshe.com/reaction/330610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantHCID 14750109HCID 14750109—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 14750110HCID 1475011081.4%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of 12.15 g (47.6 mmol) of 4-(t-butyldimethylsiloxymethyl)heptanenitrile in 120 mL of toluene at -70° C., under argon, was added 35.3 mL (53.0 mmol) of a 1.5 M solution of diisobutylaluminum hydride in toluene. After stirring at -70° C. for 3.25 hr, 36.5 mL of methanol was added and the mixture was poured into a mixture of ca. 200 mL of ether, ca. 100 g of ice and 214 mL of 3N hydrogen chloride solution. The aquenous layer was separated and extracted with 3×200 mL of ether. The combined organic layers were washed with 120 mL of saturated sodium bicarbonate solution and 120 mL of saturated brine (a gelatinous precipitate, which resulted on washing with saturated brine, was removed by filtration through celite prior to separation of the aqueous layer), dried (Na2SO4), filtered and concentrated. The residue was purified by column chromatography on silica gel to give 10.01 g (81.4%) of crude 4-(t-butyldimethylsiloxymethyl)heptanal; TLC (SiO2, 1:9 ethyl acetate:hexane) Rf 0.55 (PMA); IR (chloroform): μmax 1719 (aldehyde C=O) cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04897477
Source datasetuspto-grants-1990_01
ORD IDord-7ac0b076916d4a30b7ad5b90f095029e
Source noteuspto-grants-1990_01