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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6055Generated: October 30, 2026

Hydrochloric Acid → (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanal

https://huagongshe.com/reaction/6055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactantt-butyl (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanoateHCID 86743988—
SolventTolueneHCID 1140—
Product(R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanalHCID 14852578—

Reaction Conditions

Temperature-75 °C

Reaction Steps

I)a) 9.2 g of t-butyl (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanoate were dissolved in 115 ml of toluene while gassing with argon and with the exclusion of moisture and cooled to -75° C. 26.5 ml of a 1.2M solution of diisobutylaluminum hydride in toluene were then added dropwise in such a manner that the temperature did not exceed -70° C. After stirring at -75° C. for 1 hour there were added dropwise 7.4 ml of saturated aqueous ammonium chloride solution and subsequently 15.5 ml of 1N hydrochloric acid at -70° C. The mixture was then left to warm to room temperature. After stirring for 1 hour the organic phase was dried, filtered and evaporated. The material obtained was chromatographed on silica gel. There was obtained (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanal as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246960
Source datasetuspto-grants-1993_09
ORD IDord-3076d3da99f84c1fb207661fe9054400
Source noteuspto-grants-1993_09