Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703681Generated: November 1, 2026

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

https://huagongshe.com/reaction/703681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantAmmonium ChlorideHCID 25517—
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

(1J.a) 9.2 g of t-butyl (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanoate are 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 DIBAH solution in toluene are then added dropwise within 1/2 hour in such as manner that the temperature does not exceed -70° C. The mixture is stirred at -75° C. for a further one hour. There are then added dropwise 7.4 ml of saturated ammonium chloride solution and subsequently 15.5 ml of 1N hydrochloric acid at -70° C. The cooling bath is removed and the mixture is left to warm to room temperature. After stirring at room temperature for one hour the organic phase is separated and washed with water. The organic phase is dried, filtered and evaporated. The material obtained is chromatographed on silica gel. There is obtained [(R)-3-[(tetrahydro-2H-pyran-2-yl)oxyl]tetradecanal as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983746
Source datasetuspto-grants-1991_01
ORD IDord-7d1c028bb53e4cbca227ca28d9a605b3
Source noteuspto-grants-1991_01