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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | t-butyl (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanoate | HCID 86743988 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanal | HCID 14852578 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983746 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-7d1c028bb53e4cbca227ca28d9a605b3 |
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| Source note | uspto-grants-1991_01 |
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