HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900337Generated: October 29, 2026
Tetrahydrofuran → trans-3-[3-(1-Dodecynyl)phenyl]propen-1-ol
https://huagongshe.com/reaction/1900337
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl trans-3-[3-(1-Dodecynyl)phenyl]-2-propenoate | HCID 18373045 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | trans-3-[3-(1-Dodecynyl)phenyl]propen-1-ol | HCID 18372907 | 81.5% |
Reaction Steps
To a solution of ethyl trans-3-[3-(1-dodecynyl)phenyl]-2-propenoate (10.0 g) and dry tetrahydrofuran (100 ml) at -78° C. was added diisobutylaluminum hydride (1.5M in toluene) (49 ml) slowly. The reaction mixture was stirred for 20 mins at -78° C., and 25% sodium hydroxide solution (3 ml) was added. The mixture was slowly warmed to room temperature and an additional 25% sodium hydroxide solution (3 ml) was added. The mixture was diluted with ethyl acetate and washed with water and brine. The organic phase was separated, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was flash chromatographed over silica gel (eluted with ethyl acetate/hexane/1:3). The appropriate fractions were collected and evaporated to afford 7.14 g (81%) of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05574164 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-b9dd05a8192144f0a1dff75f15352c1d |
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| Source note | uspto-grants-1996_11 |
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